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Comparing the results of using a drain and not using a drain in mammoplasty

Comparing the results of using a drain and not using a drain in mammoplasty patients with volume reduction of less than 500 cc

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250824066966N1
Enrollment
13
Registered
2025-09-23
Start date
2025-09-23
Completion date
Unknown
Last updated
2025-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mamoplasty. Encounter for breast reconstruction following mastectomy

Interventions

Intervention 1: Intervention group: They will undergo surgery using the standard superomedial pedicle technique and short scar, and will use drains after surgery. Intervention 2: Control group: They w

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Undergoing reduction mammaplasty with a resection volume of less than ??? cc per breast. Body Mass Index (BMI) between ?? and ?? kg/m² Good general health status (ASA Class I–II) No previous breast surgery No history of breast pathology (e.g., benign or malignant tumors)

Exclusion criteria

Exclusion criteria: Simultaneous performance of other surgical procedures on the breast Resection volume greater than ??? cc per breast. History of underlying diseases such as uncontrolled diabetes, heart failure, or renal failure. Active smokers or those with a history of smoking within the past ? months History of bleeding disorders or current use of anticoagulant medications Previous history of radiotherapy or surgery involving the breast Presence of active infections or chronic wounds at the time of surgery Inability to comply with postoperative follow-up visits

Design outcomes

Primary

MeasureTime frame
Hematoma. Timepoint: Three months after surgery. Method of measurement: Ultrasound.;Seroma. Timepoint: Three months after surgery. Method of measurement: Ultrasound.;Recovery Time. Timepoint: Three months after surgery. Method of measurement: Days.;Wound dehiscence. Timepoint: Three months after surgery. Method of measurement: standard scale (0-2).;Infection. Timepoint: Three months after surgery. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlaa Aqel

Iran University of Medical Sciences

d.alaa.aqel@gmail.com+98 21 8871 7272

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026