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Redefining Limits: A Clinical Trial on the Safety of Combining Liposuction With Undermining During Abdominoplasty

Redefining Limits: A Clinical Trial on the Safety of Combining Liposuction With Undermining During Abdominoplasty

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07590492
Enrollment
63
Registered
2026-05-15
Start date
2022-07-01
Completion date
2024-03-31
Last updated
2026-05-15

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

Conditions

Abdominal Lipodystrophy, Abdominal Wall Laxity, Abdominal Wall Viability

Keywords

Abdominoplasty, Liposuction, Undermining

Brief summary

This study evaluates the safety and outcomes of combining liposuction with varying degrees of abdominal flap undermining during abdominoplasty. Patients were randomly anssigned into three groups based on the extent of undermining and use of liposuction. Outcomes assessed included complication rates, horizontal laxity, and aesthetic results.

Interventions

PROCEDURELiposuction

Liposuction of the abdominal flap

PROCEDUREWide undermining

Wide undermining of the abdominal flap

PROCEDURELimited undermining

Limited undermining of the abdominal flap

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Adult patients undergoing * Patients fit for elective surgery * BMI less than 35 kg/m2

Exclusion criteria

* Significant uncontrolled comorbidities * Previous major abdominal surgery affecting flap vascularity

Design outcomes

Primary

MeasureTime frameDescription
Aesthetic outcome6 months postoperativelyThe postoperative aesthetic outcome was assessed using four predefined criteria by three independent surgeons in a double-blinded fashion. Each patient was assigned a postoperative score, with 1 representing the poorest outcome and 5 the best outcome. The mean score of all reviewers was then calculated for each case. These criteria included waist contour, residual adiposity (central), skin flaccidity, and the overall aesthetic appearance.
Postoperative complication rate (e.g., seroma, necrosis, infection)Within 6 months postoperatively

Secondary

MeasureTime frameDescription
Horizontal laxity6 months postoperativelyThe "bury test" was used to assess the amount of horizontal laxity. The "bury test", almost the reverse of the pinch, involves burying the loose skin by tightly rolling the skin folds on either side of the resection area, and marking the maximum width of skin contact. This distance was measured both at rest and under tension.
Change in BMI6 months postoperatively
Epigastric pinch6 months postoperativelyThe epigastric pinch was measured pre and postoperatively and difference was recorded

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 16, 2026