Self-Hypnosis for the Enhanced Recovery After Surgery in Patients With Gynecologic Cancer (NCT04266886) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Self-Hypnosis for the Enhanced Recovery After Surgery in Patients With Gynecologic Cancer
United States152 participantsStarted 2018-09-11
Plain-language summary
This trial studies how well self-hypnosis works in enhancing recovery after surgery in patients with gynecologic cancer. A guided relaxation method called self-hypnosis may help affect how patients feel pain and symptoms after surgery.
Who can participate
Age range18 Years
SexFEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Undergoing an exploratory laparotomy for suspected gynecologic cancer, which includes metastatic disease from neoplasia originating in other organs
* Planned participation in the Gynecologic Enhanced Recovery Pathway
* Patient must be able to read, understand, and speak English
* Consents to being part of a randomized study
* Patient has physical and mental capabilities to take part in study
Exclusion Criteria:
* Sensitivity to amide-type local anesthetics
* Patients on long-acting opioid medications, or scheduled (four or more times a day for seven or more days) short-acting opioid medications within the last 30 days
* Emergency surgery of any type that does not allow for proper time for protocol review by the patient
* Surgery that involves known/anticipated resection of anterior abdominal wall with plastic surgery reconstruction
* Patients undergoing known/anticipated anterior abdominal wall hernia repairs
* Patients undergoing pelvic exenteration
* Patients with known major psychiatric disease
* Patients with hearing impairment such that they are unable to hear the intervention
What they're measuring
1
Feasibility of participating in pre-operative self-hypnosis