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NCT04266886 · ClinicalTrials.gov registry record · NA
Self-Hypnosis for the Enhanced Recovery After Surgery in Patients With Gynecologic Cancer
A NA study of Malignant Female Reproductive System Neoplasm and Metastatic Cervical Cancer, sponsored by M.D. Anderson Cancer Center.
- Active
- Registry status
- NA
- Development phase
- 152
- Enrollment target
- 1
- Study location
NCT04266886 is a NA study of Malignant Female Reproductive System Neoplasm and Metastatic Cervical Cancer that is active but no longer recruiting, run by M.D. Anderson Cancer Center. The registered enrollment target is 152 participants, below the 396-participant average among 18 other Malignant Female Reproductive System Neoplasm trials with a reported enrollment target (62% lower). The trial reports 1 study location across 1 state.
The verdict
NCT04266886, a NA study of Malignant Female Reproductive System Neoplasm and Metastatic Cervical Cancer, is active but no longer recruiting, sponsored by M.D. Anderson Cancer Center.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 152 participants
- Enrollment target
- 1
- Study location
Study 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.
Conditions Studied
Interventions
- OTHER Quality-of-Life Assessment
- OTHER Questionnaire Administration
- OTHER Best Practice
- PROCEDURE Hypnotherapy
Study Locations (1)
Texas
- M D Anderson Cancer Center - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 152 participants |
| Start Date | 2018-09-11 |
| Est. Completion | 2027-12-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04266886
The ClinicalTrials.gov registry entry for NCT04266886 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 152 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 396-participant average among 18 other Malignant Female Reproductive System Neoplasm trials with a reported enrollment target (62% lower). The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Malignant Female Reproductive System Neoplasm appearing as the primary indexed condition, and to 4 interventions - of which Quality-of-Life Assessment is the first listed.
NCT04266886 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT04266886 about?
NCT04266886 is a clinical study titled "Self-Hypnosis for the Enhanced Recovery After Surgery in Patients With Gynecologic Cancer". 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.
What is the current status of trial NCT04266886?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 152 participants. The study started on 2018-09-11. Estimated completion is 2027-12-31.
What conditions does trial NCT04266886 study?
This clinical trial studies the following conditions: Malignant Female Reproductive System Neoplasm, Metastatic Cervical Cancer, Recurrent Malignant Female Reproductive System Neoplasm.
What interventions are being tested in trial NCT04266886?
The interventions under investigation include: Quality-of-Life Assessment (OTHER), Questionnaire Administration (OTHER), Best Practice (OTHER), Hypnotherapy (PROCEDURE).
Who is sponsoring clinical trial NCT04266886?
This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04266886 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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