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Unilateral Laparoscopic Diathermy Adjusted to Ovarian Volume

NCT01833949 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 96

Last updated 2013-04-17

No results posted yet for this study

Summary

The objective of our study was to compare the efficiency of the right ULOD using thermal doses adjusted to ovarian volume (60 J/cm3) with the BLOD method at constant dose and to assess treatment efficiency.

Conditions

  • PCOS

Interventions

PROCEDURE

Unilateral laparoscopic drilling

Unilateral laparoscopic drilling with diathermy adjusted to ovarian volume

PROCEDURE

Bilateral laparoscopic drilling

Bilateral laparoscopic drilling with fixed doses energy

Sponsors & Collaborators

  • KBC Split

    lead OTHER

Principal Investigators

  • Martina MS Šunj, dr.med

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-09-30
Primary Completion
2013-01-31
Completion
2013-01-31

Countries

  • Croatia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01833949 on ClinicalTrials.gov