Using acupuncture to improve quality of life for women undergoing gynecological surgery
Assessing Effectiveness of Acupuncture and Integrative Care in Reducing Peri- and Intra-operative Pain and Anxiety in Patients With Gynecological Cancer: A Randomized Controlled Study
This study is testing if acupuncture can help women feel less anxious and in less pain during and after gynecological surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 135 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Carmel Medical Center Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Haifa) |
| Trial ID | NCT03560388 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of complementary and integrative medicine (CIM) treatments, particularly acupuncture, on anxiety, pain, and overall quality of life in women undergoing surgery for gynecological cancer. The approach involves administering intensive CIM treatments within 24 hours before and during the surgical procedure. The hypothesis is that these treatments will alleviate perioperative anxiety and pain, potentially reducing the need for analgesics during and after surgery. The study aims to provide insights into how integrative care can enhance patient outcomes in gynecological oncology.
Who should consider this trial
Good fit: Ideal candidates are female patients aged 18 and older who are scheduled for surgery due to suspected or established gynecological cancer.
Not a fit: Patients who are pregnant or those with chronic pain treated with opiates in the month prior to surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce anxiety and pain for patients undergoing gynecological surgery, improving their overall quality of life.
How similar studies have performed: Previous studies have shown that complementary and integrative medicine treatments can effectively improve quality of life and related symptoms in patients with gynecological cancer, suggesting a promising avenue for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: Female patients age ≥ 18 years, who were referred to surgery for suspected/established gynecological-oncology cancer at the Carmel Medical Center; Patients diagnosed with class1-3 peri-operative risk according to American Society of Anesthesia. Exclusion Criteria:Unwillingness to sign the research participation form and/or limitations in comprehending the informed consent; during pregnancy; patients with chronic pain treated with opiates within one month preceding surgery.
Where this trial is running
Haifa
- Carmel Medical center — Haifa, Israel (Recruiting)
Study contacts
- Principal investigator: Eran Ben-Arye, MD — Clalit Health Services
- Study coordinator: Eran Ben-Arye, MD
- Email: eranben@netvision.net.il
- Phone: 0528709282
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.