Skip to main content
OpenTrials
Completed

NCT Number: NCT06070363

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Suryamin Hung, Jakarta, DKI Jakarta, Indonesia

Loading trial locations.

About this study

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

  • The patient is diagnosed with gynecological cancer
  • Women over 18 years to 65 years
  • 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)
  • Willing to participate in this study and sign an informed consent Exclusion Criteria
  • 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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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
  • direct from cancer
  • Treatment proces surgery, radiotherapy, chemotherapy, paliatif treatment, supportive treatment
  • 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.

Treatment and study plan

Manual acupuncture

Other

Acupuncture Needle Insertion

Primary outcomes

  1. Pain severity with Visual Analog Scale

    Time frame: 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 outcomes

  1. Quality of Life with European Organisation for Research and Treatment of Cancer Quality of Life C30

    Time frame: 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

    Time frame: 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

Sponsors and collaborators

Lead sponsor

Indonesia University

Other

Registry information

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Oct 6, 2023
Registry last updated
Jan 29, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.