Clinical trial · Interventional
Long Term Outcomes Following Total Laparoscopic Hysterectomy and Laparoscopic Supracervical Hysterectomy
A Comparison of Long Term Outcomes Following Total Laparoscopic Hysterectomy and Laparoscopic Supracervical Hysterectomy.
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Objective: To compare the occurrence and intensity of pelvic pain as well as patient satisfaction and quality of life after total laparoscopic and laparoscopic supracervical hysterectomy. Design: Prospective randomised trial. Null hypothesis 1: There is no significant difference in occurrence and intensity of pelvic pain following TLH compared with following LSH. Null hypothesis 2: There is no significant difference in patient satisfaction and quality of life following TLH compared with following LSH.
Conditions
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Abnormal Uterine Bleeding | — | UNRESOLVED | — |
| Dysmenorrhea | — | UNRESOLVED | — |
| Fibromas | Fibroma | ALIAS | 0.90 |
| Laparoscopic Supracervical Hysterectomy | — | UNRESOLVED | — |
| Total Laparoscopic Hysterectomy | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Laparoscopic supracervical hysterectomy | Procedure | — | UNRESOLVED |
| TLH | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Total laparoscopic hysterectomy
- interventionNames
- Procedure: TLH
- type
- ACTIVE_COMPARATOR
- label
- Laparoscopic supracervical hysterectomy
- interventionNames
- Procedure: Laparoscopic supracervical hysterectomy
Primary outcomes (1)
- measure
- Pelvic pain reduction after the procedure. Occurrence and intensity of pelvic pain after the procedure.
- timeFrame
- 12 months after the procedure
- description
- 10-point visual analogue scale. Values are given as median (range), mean (sd) or n (%).
Secondary outcomes (8)
Eligibility
Eligibility (as posted)
- Sex
- Female
Show eligibility criteria text
Inclusion Criteria: * Premenopausal women who are referred to the department * benign condition requiring hysterectomy * Dysmenorrohea/cyclic pelvic pain * Informed consent Exclusion Criteria: * Women who are unable to communicate in Norwegian language. * Women with a previous history of cervical dysplasia, with cellular changes suggestive of dysplasia in preoperative cervical smear. * Women with atypical hyperplasia or malignancy in preoperative endometrial biopsy. * Women with a substantially enlarged uterus requiring abdominal hysterectomy or not suitable for TLH (\> 12 week amenorrhea). * Women with a concomitant condition requiring uni- or bilateral oophorectomy. * Postmenopausal women. * Women with no dysmenorrohea/cyclic pelvic pain (\<1 on a 10-point visual analogue scale). * Women with deep infiltrating endometriosis.
References
Publications (0)
Data not yet available