CClinicalTrials.gg
Status unknownNCT04646070Updated Nov 27, 2020

Superomedial Pedicle Versus Inferior Pedicle Techniques in Wise Pattern Reduction Mammaplasty :A Comparison Study

An interventional study of Reduction mammaplasty in To Compare Complications of Both Techniques in Wise Pattern Reduction Mammaplasty and to Correlate Between Complications and Patient Mediated Factors, sponsored by Kafrelsheikh University. Status unknown at 1 site in Egypt. Open to female participants. Per ClinicalTrials.gov, last updated 2020-11-27.

Sponsored by Kafrelsheikh University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Nov 2020), so the status shown — last known as Recruiting — may be out of date.

From the registry’s dates

  • Registered 10 months after the study started (first participant enrolled Jan 2020, registered Nov 2020).
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Sex
Female
01

Study summary

A comparison study between superomedial and Inferior pedicle techniques in wise pattern reduction mammaplasty

Read the detailed description

To compare complications of both techniques in wise pattern reduction mammaplasty and to correlate between complications and patient mediated factors

02

Conditions studied

  • To Compare Complications of Both Techniques in Wise Pattern Reduction Mammaplasty and to Correlate Between Complications and Patient Mediated Factors
03

In context

Lead sponsor

Kafrelsheikh University is the lead sponsor of 285 studies on the registry; 110 are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:

-

Exclusion Criteria:

  • previous extensive breast surgery Breast cancer
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
30 participants (estimated)

Study arms

  • Active comparator
    Wise pattern reduction mammaplasty using Inferior pedicle

    Wise pattern reduction mammaplasty using Inferior pedicle

    Procedure: Reduction mammaplasty

  • Active comparator
    Wise pattern reduction mammaplasty using superomedial pedicle

    Procedure: Reduction mammaplasty

Interventions

  • ProcedureReduction mammaplasty

    Breast reduction surgery

    Also known as: Superomedial pedicle versus Inferior pedicle techniques in wise pattern reduction mammaplasty

06

What researchers measure

Primary outcomes

  1. To compare complications of both techniques including nipple areola complex necrosis

    Complications include NAC necrosis and other minor complications including wound dehiscence and seroma or hematoma

    Time frame: 30 days postoperative

Secondary outcomes

  1. To correlate between complications and patient mediated factors

    Patient mediated factors including age, BMI, preoperative hb, suprasternal notch to nipple distance

    Time frame: 30 days postoperative

07

Study locations

1 of 1 sites recruiting
  • Kafr Elsheikh University Hospital
    Kafr Ash Shaykh, Egypt
    • Rami Ali Abdelkareem Eleiba, Master · Contact
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes

Supporting information: Study protocol, Sap

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 27, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04646070
Lead sponsor
Kafrelsheikh University
Responsible party
Rami Ali Abdelkareem Eleiba (Resident of plastic surgery, Kafrelsheikh University) — Principal investigator
First posted
Nov 27, 2020
Start date
Jan 20, 2020
Primary completion
Jan 20, 2021 (estimated)
Completion
Jan 20, 2021 (estimated)
Last update
Nov 27, 2020

Study contacts

Rami Ali Abdelkareem Eleiba, Master
Contact
Ramieleiba@gmail.com
+2 01028835799
Safwat Adel hegazy, MD
study director · Kafr Elsheikh University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Nov 2020. You cannot join it, but the record below documents what was studied.

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