Clinical trial · Interventional
Comparison Between Robotic (RM) and Laparoscopic Myomectomy (LM)
Comparison Between Robotic (RM) and Laparoscopic Myomectomy (LM): a Multicenter Randomized Trial (RoLM Trial)
NCT04282863CI-TRIAL-00043635unknownN/AClinicalTrials.gov clinicaltrialsProvenance
- 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)
This is a single-blinded RCT evaluating the effect of robotic-assisted (RM) or conventional laparoscopic surgery (LM) in the management of uterine leiomyomas.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Surgical Procedure, Unspecified | — | UNRESOLVED | — |
| Uterine Leiomyoma | Uterine Corpus Leiomyoma | ALIAS | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| LM | Procedure | — | UNRESOLVED |
| RM | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- robotic-assisted laparoscopic myomectomy (RM)
- description
- After randomization, participants who are assigned to the robotic-assisted laparoscopic myomectomy (RM) agree to receive RM.
- interventionNames
- Procedure: RM
- type
- PLACEBO_COMPARATOR
- label
- Conventional laparoscopic myomectomy (LM)
- description
- After randomization, participants who are assigned to the Conventional laparoscopic myomectomy (LM) agree to receive LM.
- interventionNames
- Procedure: LM
Primary outcomes (1)
- measure
- Conversion rate
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 20 Years
Show eligibility criteria text
Inclusion Criteria: * All women who has symptomatic benign myoma. Exclusion Criteria: * Patient is unwilling the scheduled operation after randomization.
References
Publications (0)
Data not yet available
No reference posted for this study.