Clinical trial · Interventional
Temporary Simultaneous Two-arterial Occlusions During Laparoscopic Myomectomy
Temporary Simultaneous Two-arterial Occlusions to Reduce Operative Blood Loss During Laparoscopic Myomectomy: a Randomized Controlled Trial
NCT02747550CI-TRIAL-00037889TESTOcompletedN/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 of this study was to evaluate the efficacy and safety of the temporary simultaneous two-arterial occlusions (TESTO) on operative blood loss during laparoscopic myomectomy.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Myoma | Myoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| LM without TESTO | Procedure | — | UNRESOLVED |
| LM with TESTO | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- LM with TESTO
- description
- In subjects allocated to the experimental group, the temporary simultaneous two-arterial occlusions (TESTO) procedure was performed to minimize operative blood loss during laparoscopic myomectomy.
- interventionNames
- Procedure: LM with TESTO
- type
- ACTIVE_COMPARATOR
- label
- LM without TESTO
- description
- In the control group, no intervention for the temporary simultaneous two-arterial occlusions (TESTO) procedure was made during laparoscopic myomectomy.
- interventionNames
- Procedure: LM without TESTO
Primary outcomes (1)
- measure
- operative blood loss
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 19 Years
- Maximum age
- 48 Years
Show eligibility criteria text
Inclusion Criteria: * women with symptomatic myomas such as menorrhagia, pelvic pressure/pain, or infertility * women who were planning to undergo laparoscopic myomectomy * women who had ≤ 10 myomas, with the largest myoma ≤ 10 cm * women with regular menstrual bleeding * women who were not pregnant at the surgery * women between 19 and 48 years of age. Exclusion Criteria: * women who underwent concomitant complex surgical procedures at the time of laparoscopic myomectomy, such as severe adhesiolysis or resection for severe endometriosis * women who were in postmenopausal or climacteric status * women with a history of oophorectomy or salpingo-oophorectomy * women with any suggestion of malignant uterine or adnexal diseases * women with major medical comorbidities or psychiatric illnesses, which could affect follow-up and/or compliance * women who refused to participate or give consent to the procedures
References
Publications (0)
Data not yet available
No reference posted for this study.