Dexmedetomidine,Ketamine and Their Combination to Bupivicaine on Thoracic Epidural Analgesia

Sponsor
Assiut University (Other)
Overall Status
Completed
CT.gov ID
NCT03063671
Collaborator
(none)
20
1
4
14.9
1.3

Study Details

Study Description

Brief Summary

This study investigate the effect of addition dexmedetomidine, ketamine or their combination to bupivacaine in thoracic epidural analgesia on acute postoperative pain after breast cancer surgery.

Condition or Disease Intervention/Treatment Phase
  • Drug: Ketamine, bupivacine,dexmedetomidine
Phase 2/Phase 3

Detailed Description

Breast cancer is the most common cancer diagnosed in Egyptian women. Many modalities are used in the treatment of breast cancer including chemotherapy, radiotherapy or surgical intervention. Nowadays, surgical intervention is more conservative.Modified radical mastectomy (MRM) is the standard surgical procedure of choice in these patients. MRM is usually performed under general anesthesia, almost always combining intravenous and inhalational agents.The drawback of general anesthesia includes inadequate pain control due to lack of analgesia, high incidence of nausea and vomiting, stress of anesthesia and surgery, and increasing the length of hospital stay.Post mastectomy pain is a pain which occur following breast cancer procedures, particularly those operations that remove tissues in upper outer quadrant of breast and/or axilla. This pain can be severe enough to cause long term disabilities and interfere with sleep, performance of daily activities. Also, it can seriously affect the patient mood, and social functions.

Thoracic epidural analgesia (TEA) faces growing interest as adjuvant anesthetic and post-operative analgesic regimen. the use of adjuvant drug with local anesthetic is essential as it prolongs the duration of action, gives better success rate and increases patient satisfaction.

Ketamine, an N-methyl-D-aspartate (NMDA) antagonist, not only abolishes peripheral afferent noxious stimulation, but it can also prevent the central sensitization of nociceptors. When added to epidural local anesthetics, ketamine appears to have adjuvant effects. Dexmedetomedine is a selective, α2-adrenoceptor agonist with analgesic potency, sedative properties, and minimal respiratory depression when used as an adjuvant to regional anesthesia.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Effect of Adding Dexmedetomidine, Ketamine and Their Combination to Bupivicaine in Thoracic Epidural Analgesia on Post-mastectomy Pain
Actual Study Start Date :
Jan 1, 2017
Actual Primary Completion Date :
Jul 1, 2017
Actual Study Completion Date :
Apr 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: bupivacine group

preoperative insertion of thoracic epidural at T4-5 and adminstration of 12 ml bupivacine 0.125% as one shot 15 minutes before general anesthesia postoperative analgesia done by infusion of bupivacaine 0.125% (5ml/hour through thoracic epidural catheter for 12 hours).

Drug: Ketamine, bupivacine,dexmedetomidine
thoracic epidural catheter insertion at T4-5

Active Comparator: ketamine group

preoperative insertion of thoracic epidural at T4-5 and adminstration of 12 ml bupivacine 0.125% plus ketamine in a dose 0.5 mg/kg 15 minutes before general anesthesia postoperative analgesia will be preformed by infusion of mixture of (bupivacaine 0.125% plus ketamine 0.5 mg/ml ml) in a rate of 5ml/hour through thoracic epidural catheter for 12 hours

Drug: Ketamine, bupivacine,dexmedetomidine
thoracic epidural catheter insertion at T4-5

Active Comparator: dexmedetomidine group

preoperative insertion of thoracic epidural at T4-5 and adminstration of 12 ml bupivacine 0.125% plus dexmedetomidine in a dose 1 ug/kg 15 minutes before general anesthesia Postoperative analgesia will be performed using infusion of mixture of (bupivacaine 0.125% plus dexmedetomedine 2μg/ ml) in a rate of 5ml/hour through thoracic epidural catheter for 12 hours.

Drug: Ketamine, bupivacine,dexmedetomidine
thoracic epidural catheter insertion at T4-5

Active Comparator: ketamine-dexmedetomidine group

preoperative insertion of thoracic epidural at T4-5 and adminstration of 12 ml bupivacine 0.125% plus both ketamine in a dose 0.3 mg/kg and dexmedetomidine in a dose 0.1 ug/kg 15 minutes before general anesthesia Postoperative analgesia will be performed using infusion of mixture of (bupivacaine 0.125% plus dexmedetomedine 2μg/ ml and and ketamine 0.5 mg/ml) in a rate of 5ml/hour through thoracic epidural catheter for 12 hours.

Drug: Ketamine, bupivacine,dexmedetomidine
thoracic epidural catheter insertion at T4-5

Outcome Measures

Primary Outcome Measures

  1. total dose of intravenous morphine consumption in the first 48 hours post operatively [48 hours postoperative]

    total dose of intravenous morphine comsumption

Secondary Outcome Measures

  1. Visual analogue scale [0, 2,4,6,8,18,36,48 hours]

    Visual analogue scale will be assessed at rest and on movement (abduction of the ipsi-lateral arm).

  2. MAP [0,30,60,120,150 minutes]

    mean arterial blood pressure

  3. HR [0,30,60,120,150 minutes]

    heart rate

  4. sedation score [0, 2,4,6,8,18,36,48 hours]

    sedation sore using sedation scale where; 0 = aware - 1 = drowsy - 2 = asleep/easily respond to verbal command - 3 = asleep/difficulty responding to verbal command -4 = asleep/no respond to verbal command

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 70 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients scheduled for modified radical mastectomy.

  • ASA Physical status I, II and III.

Exclusion Criteria:
  • Patients' refusal.

  • Uncooperative patients & severe psychiatric illness (cannot evaluate their own pain intensity using visual analogue scale (VAS).

  • Patients with history of drug allergy.

  • severe renal or liver impairment, unstable ischemic heart disease

  • Any contraindications to epidural analgesia (coagulopathy, recent -less than 1 week-treatment with thrombolytic or potent antiplatelet drugs as clopidogrel, and local infection).

Contacts and Locations

Locations

Site City State Country Postal Code
1 south Egypt cancer institute Assuit Egypt

Sponsors and Collaborators

  • Assiut University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Shereen Mamdouh, lectruer, Assiut University
ClinicalTrials.gov Identifier:
NCT03063671
Other Study ID Numbers:
  • 110
First Posted:
Feb 24, 2017
Last Update Posted:
Jun 28, 2019
Last Verified:
Jun 1, 2019
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Shereen Mamdouh, lectruer, Assiut University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 28, 2019