Effectiveness of Manual Acupuncture and Standard Therapy Compared to Standard Therapy in Gynecological Cancer Pain

Sponsor
Indonesia University (Other)
Overall Status
Recruiting
CT.gov ID
NCT06070363
Collaborator
(none)
58
1
2
3.1
18.8

Study Details

Study Description

Brief Summary

Cancer patients experience cancer pain as much as 66%. Cancer pain is pain that occurs in patients with neoplastic/malignancy and the source of the pain can come from malignant processes, treatments such as radiotherapy, chemotherapy, and surgery as well as other causes that are not related to malignancy processes. Unresolved pain can reduce the quality and life expectancy of cancer pain patients. The prevalence of cancer itself in Indonesia, the case of cervical cancer itself ranks second after breast cancer. In recent decades, acupuncture analgesics have been widely used to relieve cancer pain, and can also reduce the dose and side effects of analgesics. However, substantially the use of acupuncture in cancer pain is still very rare.

Condition or Disease Intervention/Treatment Phase
  • Other: Manual Acupuncture
N/A

Detailed Description

The main outcome is to analyze the effectiveness of manual acupuncture therapy (LI4,PC6, LR3,ST36, and SP6 plus standard therapy on pain intensity (VAS score), changes in analgesic dose, and quality of life (QLQ C-30 EORTC score) in patients with gynecological cancer pain compared to standard therapy alone.

The patient will attempt 3-day manual acupuncture therapy with seven days follow up Patient will receive acupuncture therapy daily for 3 days, for 15 minute each day.

The research design in this study was a single-blinded randomized control clinical trial. With outcome measures for

With Subject criteria:

Inclusion Criteria

  1. The patient is diagnosed with gynecological cancer

  2. Women over 18 years to 65 years

  3. Subjects experiencing cancer pain, with VAS ≥4, namely pain caused by:

  • tumors,

  • before or during a therapeutic process (radiation therapy, chemotherapy, or post-surgery)

  • side effect or the result of toxicity of cancer treatment

  • Supportive therapy (palliative therapy, painkillers, antidepressants)

  1. Willing to participate in this study and sign an informed consent Exclusion Criteria
  1. The patient has a medical emergency / hemodynamically unstable 2) Patients with contraindications for manual acupuncture procedures such as wounds and infections at the point where the puncture will be performed, patients allergic to stainless steel62 3) Uncooperative patients (patients with negative and aggressive affect, who do not allow acupuncture therapy) 4) There is a tumor in the area that will be stabbed and stimulated in the pregnant woman's abdomen, close to the heart, or around the carotid sinus, lymphedema, needle insertion into the prosthesis 5) Patients with heart rhythm disorders 6) The patient uses a pacemaker 7) Patients with disorders of the auricle such as eczema, external otitis, and psoriasis 8) Patients with blood clotting disorders, with platelets <50,000, and in neutropenic conditions with neutrophils <1000

Study Design

Study Type:
Interventional
Anticipated Enrollment :
58 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
The investigator blind the participant allocation
Primary Purpose:
Supportive Care
Official Title:
Effectiveness of Manual Acupuncture and Standard Therapy Compared to Standard Therapy in Gynecological Cancer Pain
Actual Study Start Date :
Aug 29, 2023
Anticipated Primary Completion Date :
Nov 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control

The Patient are cancer patient that experience cancer pain that only receive analgetic drug treatment according to WHO Stepledder of Pain

Experimental: Manual acupuncture and standard Therapy

The Patient are cancer patient that experience cancer paint that receive analgetic drug treatement according WHO stepledder of pain and receive manual acupuncture

Other: Manual Acupuncture
Acupuncture Needle Insertion

Outcome Measures

Primary Outcome Measures

  1. Pain severity with Visual Analog Scale [Before treatment, After treatment in day 1, day 2, day 3, day 5 and day 7]

    Visual Analog Scale (VAS) that score 0 is no pain to 100 the worse pain A higher scale means worse outcomes

Secondary Outcome Measures

  1. Quality of Life with European Organisation for Research and Treatment of Cancer Quality of Life C30 [before treatment and 7 day after treatment]

    European Organisation for Research and Treatment of Cancer Quality of Life C30, that include two item of review functional scale and the global health scale both scale the higher the score the outcome will be better

  2. Analgetic Usage in dosage and frequency [Before treatment, After treatment in day 1, day 2, day 3, day 5 and day 7]

    Description of analagetic dosage and frequency during observation that will be describe as medicine category opioid non opioid, dosage and frequency

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Female 18 to 65 years old

  • Gynecocal cancer with pain ≥ 4 acording Visual Analog scale and receive analgetic medicine

  • The pain cause by

  1. direct from cancer

  2. Treatment proces surgery, radiotherapy, chemotherapy, paliatif treatment, supportive treatment

  3. Adverse reaction form treatment and intoxication

Exclusion Criteria:
  • emergency case patient with hemodynamic instable

  • patient with uncooperative behavior because ith serious psychological disorders, no currently undergoing psychiatric treatment, aggressive behavior, that not allowed for acupuncture.

  • Patients with blood clotting disorders, with platelets <50.000 and in neutropenic condition with <1000 neutrophils.

The patient has an allergy to stainless steel acupuncture needles. Wounds at the acupuncture point puncture sites, skin infections in the ears. On patients with eczema on the ears, external otitis or psoriasis.

There is a tumor in the area that will be stabbed and stimulated in the stomach pregnant women, close to the heart, or in the area of the carotid sinus lymphedema, insertion into the prosthesis.

Patients with heart rhythm disorders. The patient uses a pace maker.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Suryamin Hung Jakarta DKI Jakarta Indonesia 14250

Sponsors and Collaborators

  • Indonesia University

Investigators

  • Study Director: Suryamin Suryamin, Indonesia University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Suryamin Suryamin, Medical Doctor, Indonesia University
ClinicalTrials.gov Identifier:
NCT06070363
Other Study ID Numbers:
  • 23-06-1047
First Posted:
Oct 6, 2023
Last Update Posted:
Oct 6, 2023
Last Verified:
Aug 1, 2023
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 Suryamin Suryamin, Medical Doctor, Indonesia University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 6, 2023