Clinical trial · Interventional
Temporary Clipping of the Uterine Arteries During Laparoscopic Myomectomy
Reduction of Intraoperative Blood Loss During Laparoscopic Myomectomy by Temporary Clipping of the Uterine Arteries
NCT01530802CI-TRIAL-00006242completedN/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)
The aim is to verify, whether intraoperative temporary clipping of the uterine vessels with vascular clips can reduce blood loss significantly.
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 |
|---|---|---|---|
| Laparoscopic Myomectomy | — | UNRESOLVED | — |
| Leiomyoma | Leiomyoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| clipping of uterine arteries during laparoscopic myomectomy | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Uterine artery clipped
- description
- Both uterine arteries are temporarily clipped by Yasargil clips during laparoscopic myomectomy.
- interventionNames
- Procedure: clipping of uterine arteries during laparoscopic myomectomy
- type
- NO_INTERVENTION
- label
- Control group
- description
- Conventional laparoscopic myomectomy is performed. (No intervention to temporarily occlude uterine arteries is made)
- interventionNames
- Procedure: clipping of uterine arteries during laparoscopic myomectomy
Primary outcomes (1)
- measure
- Blood loss during laparoscopic myomectomy
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 50 Years
Show eligibility criteria text
Inclusion Criteria: * Patients are eligible for the study when between 18 and 50 years of age, * diagnosed with either symptomatic or asymptomatic leiomyomata, and with desire to keep the uterus, and whose leiomyomata had a minimal combined diameter of ≥ 4 cm. Exclusion Criteria: * patients with severe accompanying medical problems, or * with psychiatric illnesses, which jeopardize the participation, or * undergoing treatment affecting coagulation and/or hematopoiesis, and * patients with suspected malignancy.
References
Publications (0)
Data not yet available
No reference posted for this study.