- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07314086
A Clinical Effectiveness Study of Total Laparoscopic Subcutaneous Gland Resection Combined With Nipple-Areola Complex Lift in the Management of Moderate to Severe Gynecomastia in Males
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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-
Heilongjing
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Harbin, Heilongjing, China, 150001
- First Affiliated Hospital of Harbin Medical University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
(1) Those with bilateral breast development confirmed by preoperative ultrasound examination; (2) For bilateral developed breasts, the preoperative classification according to Simon's system (hereinafter referred to as Simon classification) is all at grade IIA or above.
Exclusion Criteria:
(1) Benign and malignant tumors of the male breast; (2) Other diseases such as testicular tumors, congenital testicular dysplasia syndrome, hyperthyroidism, liver cirrhosis, primary gonadal hypofunction and oral medications can lead to secondary male breast development; (3) Patients with severe primary diseases such as cardiovascular and cerebrovascular diseases, liver and kidney diseases, and coagulation disorders are not suitable for anesthesia and surgery; (4) Patients with incomplete clinical case data.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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experimental group
the group undergoing laparoscopic surgery combined with NAC lift
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control group
the group undergoing simple laparoscopic surgery
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Differences in the clinical index between the two groups
Time Frame: Baseline
|
The patients were divided into two groups: laparoscopic surgery in conjunction with NAC lift group,isolated laparoscopic surgery group.
IBM SPSS 27.0 software was used for statistical analysis.
The analysis attempt to reveal the differences between the two groups in terms of surgical time, blood loss, and drainage tube placement duration
|
Baseline
|
|
Difference in the pre- and postoperative convexity of breast between the two groups
Time Frame: Baseline
|
The patients were divided into two groups: laparoscopic surgery in conjunction with NAC lift group,isolated laparoscopic surgery group.
IBM SPSS 27.0 software was used for statistical analysis.
The analysis attempt to reveal the differences between the two groups in terms of the pre- and postoperative convexity of breast
|
Baseline
|
|
Difference in the recovery rate of skin flatness between the two groups
Time Frame: Baseline
|
The patients were divided into two groups: laparoscopic surgery in conjunction with NAC lift group,isolated laparoscopic surgery group.
IBM SPSS 27.0 software was used for statistical analysis.
The analysis attempt to reveal the differences of the recovery rate of skin flatness between the group undergoing laparoscopic surgery combined with NAC lift and he group undergoing simple laparoscopic surgery at 3, 6, and 12 months postoperatively
|
Baseline
|
|
Difference in the positioning of the NAC between the two groups
Time Frame: Baseline
|
The patients were divided into two groups: laparoscopic surgery in conjunction with NAC lift group,isolated laparoscopic surgery group.
IBM SPSS 27.0 software was used for statistical analysis.
The analysis attempt to reveal the differences between the two groups in terms of the positioning of the NAC
|
Baseline
|
|
Differences in the postoperative patient satisfaction between the two groups
Time Frame: Baseline
|
The patients were divided into two groups: laparoscopic surgery in conjunction with NAC lift group,isolated laparoscopic surgery group.
IBM SPSS 27.0 software was used for statistical analysis.
The analysis attempt to reveal the differences between the two groups in terms of postoperative patient satisfaction
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Differences in the postoperative complications between the two groups
Time Frame: baseline
|
The patients were divided into two groups: laparoscopic surgery in conjunction with NAC lift group,isolated laparoscopic surgery group.
IBM SPSS 27.0 software was used for statistical analysis.
The analysis attempt to reveal the differences between the two groups in terms of the postoperative complications
|
baseline
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20251129
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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