Clinical trial · Interventional
To Compare to 2-channel and Multiple-channel Single Port Laparoscopic-assisted Vaginal Hysterectomy
Prospective Cohort Study to Compare to 2-channel and Multiple Channel Single Port Laparoscopic-assisted Vaginal Hysterectomy
NCT01564602CI-TRIAL-00006638unknownN/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 main objective of this trial is to assess the efficacy and safety of single port-access laparoscopic-assisted vaginal hysterectomy. The operative time, weight of the uterus, blood loss and hospital stay will be record, respectively. The pain score is based on the visual analogue scale in which patients record the intensity of their pain 12, 24, and 48 hours after surgery.
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 |
|---|---|---|---|
| Adenomyosis | — | UNRESOLVED | — |
| Myoma | Myoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| comparison multiple channel port laparoscopic surgery | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- single port laparoscopic surgery
- description
- 2-channel or multiple channel single port laparoscopic surgery in gynecologic disorders
- interventionNames
- Device: comparison multiple channel port laparoscopic surgery
Primary outcomes (1)
- measure
- The operative time
- timeFrame
- We will follow the patients until one month after the surgery.
- description
- We will follow the patients until one month after the surgery. The primary outcome measure of this trial is the effect and safety of single port-access laparoscopic-assisted vaginal hysterectomy.
Secondary outcomes (4)
- measure
- weight of the uterus
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- Female
Show eligibility criteria text
Inclusion Criteria: * Patients receive laparoscopic-assisted vaginal hysterectomy (LAVH) * American Society of Anesthesiologists (ASA) physical status of patient: classification I-II Exclusion Criteria: * The procedure will be required to conversion to laparotomy. * Any cardio-vascular diseases. * Malignant disease
References
Publications (0)
Data not yet available
No reference posted for this study.