Acupuncture Effect on Digestion in Critically Ill Post-Operative Oral and Hypo-pharyngeal Cancer Patients

Sponsor
China Medical University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT03934294
Collaborator
(none)
28
1
2
22.1
1.3

Study Details

Study Description

Brief Summary

Background: Head and neck cancer patients are in high risk to suffer from malnourishment, a risk that increase in postoperative condition and with the use of enteral nutrition (EN). Until now patients who are suffering from indigestion in the ICU received treatment in the form of prokinetic drugs, drags that can lead to serious side effects and only can partially improve digestion. Acupuncture was used successfully in several clinical trials to improve postoperative indigestion in cancer patients without any reported adverse events. This study aims is to design a double blind settings in order to investigate acupuncture effect in combination of prokinetic drugs in the prevention of indigestion in postoperative oral and hypo-pharyngeal cancer patients in the Intensive Care Unit (ICU).

Methods: Single center, double blind randomize control trial will compare between two equal groups. A total of 28 patients that will meet the inclusion criteria: Age 30-80, Post plastic surgery for oral cancer or hypo-pharyngeal cancer, Apache score below 20 needed EN. Patients will be randomly divided into specific acupuncture (ACU) or non-specific acupuncture (CON) for 3 treatments in 3 days by a blind acupuncturist along with prokinetic drugs. The main outcome measurement will be the amount of days a patient need to reach Total Energy Expenditure (TEE).

Expected outcome: The results will shed light on the effectiveness and safety of acupuncture in a double blind design for posts-surgery ICU cancer patients. In addition, the study presents a revolutionary double blind design that if will prove as successful might influence the way double blind acupuncture studies are performed today.

Condition or Disease Intervention/Treatment Phase
  • Other: Specific acupuncture group
  • Drug: Metoclopramide 10mg
  • Other: Non-specific acupuncture group
N/A

Detailed Description

Background: Head and neck cancer patients are in high risk to suffer from malnourishment, a risk that increase in postoperative condition and with the use of enteral nutrition (EN). Until now patients who are suffering from indigestion in the ICU received treatment in the form of prokinetic drugs, drags that can lead to serious side effects and only can partially improve digestion. Acupuncture was used successfully in several clinical trials to improve postoperative indigestion in cancer patients without any reported adverse events. This study aims is to design a double blind settings in order to investigate acupuncture effect in combination of prokinetic drugs in the prevention of indigestion in postoperative oral and hypo-pharyngeal cancer patients in the Intensive Care Unit (ICU).

Methods: Single center, double blind randomize control trial will compare between two equal groups. A total of 28 patients that will meet the inclusion criteria: Age 30-80, Post plastic surgery for oral cancer or hypo-pharyngeal cancer, Apache score below 20 needed EN. Patients will be randomly divided into specific acupuncture (ACU) or non-specific acupuncture (CON) for 3 treatments in 3 days by a blind acupuncturist along with prokinetic drugs. The main outcome measurement will be the amount of days a patient need to reach his Total Energy Expenditure (TEE).

Expected outcome: The results will shed light on the effectiveness and safety of acupuncture in a double blind design for posts-surgery ICU cancer patients. In addition, the study presents a revolutionary double blind design that if will prove as successful might influence the way double blind acupuncture studies are performed today.

Other information: The study will be conducted in the surgical ICU department, of china medical university hospital, Taichung 404, Taiwan. The study in conducted on stable ICU patients and is anticipated to have a minimum risk for adverse events. Patients enrollment and data collection will start immediately after china medical hospital research ethics committee approval. The study expected completion time: June 2021

Study Design

Study Type:
Interventional
Actual Enrollment :
28 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
two groups, randomized, pre-post intervention studytwo groups, randomized, pre-post intervention study
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description:
Patients will be randomized to one of two groups: Acu/ Con in a 1:1 ratio. The random number and patient name will be written down on an non transparent envelope by a study nurse. The study nurse will provide an envelope containing a sheet depicting the acupoint name, location and picture (Acu / Con) to the acupuncture doctor. Acupuncture doctor (blind) will preform acupuncture on the points. 30 minutes after needle insertion, acupuncture doctor will withdraw the needles. Acupuncturists, ICU nurses, ICU doctors, researchers and statisticians will all be blind to group allocation and to the meaning of the random numbers until all acupuncture treatments have been completed.
Primary Purpose:
Treatment
Official Title:
Acupuncture Effect on Digestion in Critically Ill Post-Operative Oral and Hypo-pharyngeal Cancer Patients: A Protocol for Double Blind Randomized Control Trial
Actual Study Start Date :
May 15, 2019
Actual Primary Completion Date :
Mar 19, 2021
Actual Study Completion Date :
Mar 19, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Treatment group: specific acupuncture group(Acu)

In addition to routine ICU treatments, patients in the specific acupuncture group will also receive daily bilateral traditional Chinese medicine style acupuncture on the following acupuncture points: ST36 (Zu San Li), ST37 (Shangjuxu), ST39 (Xiajuxu), PC6 (Nei Guan) and LI4 (He Gu). The acupoints indications in this group are specific to treat indigestion related conditions. The treatment will take place once a day, over three days, for a total of three treatments. A total of 10 Needles will be used in each session Acupuncture treatment will be performed with sterile needles manufactured by "Yu Kuang" acupuncture needles 40mm with 30G. Acupuncture doctor will disinfect the acupoints with alcohol and will perform acupuncture on the marked points with needle Needle retention time will be 30 minutes. The needles will be withdrawn by acupuncture doctor.

Other: Specific acupuncture group
In addition to routine ICU treatments, patients in the specific acupuncture group will also receive daily bilateral traditional Chinese medicine style acupuncture on the following acupuncture points: ST36 (Zu San Li), ST37 (Shangjuxu), ST39 (Xiajuxu), PC6 (Nei Guan) and LI4 (He Gu). The acupoints indications in this group are specific to treat indigestion related conditions. The treatment will take place once a day, over three days, for a total of three treatments. A total of 10 Needles will be used in each session Acupuncture treatment will be performed with sterile needles manufactured by "Yu Kuang" acupuncture needles 40mm with 30G.
Other Names:
  • Specific acupuncture to treat indigestion
  • Drug: Metoclopramide 10mg
    Patients in all groups will receive Metoclopramide 10mg/ per 8 hours in the case of poor digestion, alongside the individualized drug treatment prescribed by the ICU medical doctor as per individual patient needs.
    Other Names:
  • Metoclopramide 10mg/ per 8 hours in the case of poor digestion
  • Placebo Comparator: Control group: non-specific acupuncture group (Con-Acu)

    Patients' in the non-specific acupuncture group (Con-Acu) will receive routine ICU treatment as well as a total of 3 daily non digestion related Traditional Chinese medicine style acupuncture treatments at the following acupoints: LI 15 (Jianyu), SJ 14 (JianLiao) LU3 (Tianfu), GB35 (Yangjiao), BL 59 (Fuyang). The selected control points are not indicated for the treatment of digestion related pathologies, and are not reported to improve digestive function. Acupuncture doctor 1 will disinfect the marked acupoints with alcohol and will perform acupuncture on the marked points. Needle retention time will be 30 minutes. The needles will be withdrawn by acupuncture doctor

    Drug: Metoclopramide 10mg
    Patients in all groups will receive Metoclopramide 10mg/ per 8 hours in the case of poor digestion, alongside the individualized drug treatment prescribed by the ICU medical doctor as per individual patient needs.
    Other Names:
  • Metoclopramide 10mg/ per 8 hours in the case of poor digestion
  • Other: Non-specific acupuncture group
    Patients' in the non-specific acupuncture group (Con-Acu) will receive routine ICU treatment as well as a total of 3 daily non digestion related Traditional Chinese medicine style acupuncture treatments at the following acupoints: LI 15 (Jianyu), SJ 14 (JianLiao) LU3 (Tianfu), GB35 (Yangjiao), BL 59 (Fuyang). The selected control points are not indicated for the treatment of digestion related conditions, and are not reported to improve digestive function.
    Other Names:
  • Non specific acupuncture to treat indigestion
  • Outcome Measures

    Primary Outcome Measures

    1. Time to reach Total Energy Expenditure [Up to 1 month]

      Number of days in takes for each patient to achieve the Total Energy Expenditure

    Secondary Outcome Measures

    1. Amount of prokinetic drugs prescribed [Up to 1 month]

      Secondary outcomes measures are the amount of prokinetic drugs prescribed by the ICU doctor in total dosage

    2. The need of naso-jejunal feeding tube [Up to 1 month]

      After 5 days of conservative treatment for the poor digestion (naso-gastric tube drainage of more than 500ml per day or severe diarrhea of more than 1000 ml per day)

    3. The need of parental nutrition [up to 1 month]

      In patients who cannot digest with daily naso-gastric tube drainage of more than 500ml per day or severe diarrhea of more than 1000 ml per day

    4. Incidents of vomits [Up to 1 month]

      Incidents of vomits in total number of times and volume in micro liters

    5. Albumin blood levels [Up to 1 month]

      Patient's Albumin blood levels will help to assets patient's nutrition status

    6. Total ICU stay [Up to 23 month]

      Total ICU stay in days

    7. Total hospital stay [Up to 23 month]

      Total hospital stay in days

    8. Total mechanical ventilation in days [Up to 23 month]

      A day of mechanical ventilation is at least 6 hours of mechanical ventilation in one day

    9. Total mortality [Up to 23 month]

      In case of mortality ,total mortality will be compered between the two groups

    10. Incidents of diarrhea [Up to 1 month]

      Incidents of diarrhea in number of times and volume in micro liters

    11. Incidents of constipation [Up to 1 month]

      No stool passage in 3 days will be considered as constipation

    12. Incidents of nausea [Up to 1 month]

      Incidents of nausea in number of times , measured by patient complains

    13. Incidents of gastrointestinal bleeding [Up to 1 month]

      Positive occult blood test of the naso-gastric tube drainage and in the stool

    14. Incidents of fever episodes [Up to 1 month]

      Body temperature more than 38 degrees Celsius

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    30 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age 30-80

    • Apache score below 20

    • Patients needed EN

    • Post plastic surgery, including oral cancer or hypo-pharyngeal cancer

    Exclusion Criteria:
    • Coagulopathy,

    • prolong prothrombin time (PPT) activated partial thromboplastin time (aPTT) more then 4 times

    • Thrombocytopenia - low platelet count

    • Clinically unstable: receiving two inotropic agents or Fraction of inspired Oxygen (FiO2) >70%

    • Estimated ICU stay - less than 3 days

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 surgical and burn intensive care departments and the plastic surgical department of China Medical University Hospital in Taichung city, Taiwan. Taichung City Taichung Taiwan 40402

    Sponsors and Collaborators

    • China Medical University Hospital

    Investigators

    • Principal Investigator: Pei-Yu Kao, M.D., China Medical University Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    China Medical University Hospital
    ClinicalTrials.gov Identifier:
    NCT03934294
    Other Study ID Numbers:
    • CMUH108-REC2-037(AR-1)
    First Posted:
    May 1, 2019
    Last Update Posted:
    Mar 24, 2021
    Last Verified:
    Mar 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by China Medical University Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 24, 2021