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The effect of diathermy setting on post-operative seroma following abdominoplasty

The effect of diathermy setting on post-operative seroma following abdominoplasty

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12623000322639
Enrollment
195
Registered
2023-03-27
Start date
2023-03-30
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

None listed

Brief summary

Abdominoplasty is one of the most common plastic surgery procedures performed in Australia. A common complication of abdominoplasty is the formation of post operative seroma, which is thought to be influenced by dissection technique utilised by the surgeon. We propose to conduct a study of patients undergoing abdominoplasty, comparing seroma rates with three different diathermy settings. The proposal will be a prospective, randomised, study of consecutive patients undergoing abdominoplasty, with no exclusion criteria. Only patients consenting to involvement will be included. For excision of tissue and dissection of flaps, a monopolar coagulation diathermy with power setting of 20W will be used for one group, a monopolar coagulation diathermy with power setting of 35W will be used in the second group, and a monopolar cutting diathermy with power setting of 35W will be used for the third group. All three diathermy settings are well within usual range of setting used for diathermy and pose negligible additional risk to patients in either group. We hypothesize that the lower diathermy and cutting settings will result in lower seroma rates, due to less soft tissue damage during dissection. The general surgical technique involves scalpel skin incision, monopolar dissection, liposuction, rectus divarification repair where indicated, and layered soft tissue closure. Compression garment’s will be placed at the conclusion of surgery and continued fulltime for 6 weeks. Patient demographic factors and surgical technique baseline characteristics will be compared. Drains will be emptied at midnight daily by ward nurses who are blinded to the study, with outputs documented at 24-hour intervals. Postoperative mobilisation commences on day 1, with a physiotherapist. Drains will be removed when they were <30ml/d for 2 consecutive days. Data collected will include: baseline demographics, surgical technique, daily drain outputs, time to removal of drains, development of postoperative complications. If complications include seroma or haematoma, the size, location and subsequent management will be noted. Follow up period for the purpose of this study will be 6 weeks post operatively.

Interventions

Patients included will be those consenting patients who are undergoing abdominoplasty, with the intervention/technique compared being the diathermy setting used during the operation. For excision of tissue and dissection of abdominoplasty flaps, a monopolar coagulation diathermy with power setting of 20W will be used for one group, whilst a monopolar coagulation diathermy with power setting of 35W will be used in the second group, and a monopolar cutting diathermy with power setting of 35W will

Patients included will be those consenting patients who are undergoing abdominoplasty, with the intervention/technique compared being the diathermy setting used during the operation. For excision of tissue and dissection of abdominoplasty flaps, a monopolar coagulation diathermy with power setting of 20W will be used for one group, whilst a monopolar coagulation diathermy with power setting of 35W will be used in the second group, and a monopolar cutting diathermy with power setting of 35W will be used for the third group Diathermy will be used throughout the dissection portion of the abdominoplasty (excising out skin and raising abdominal flaps). This is estimated to be the first 30 minutes of the operation. The same 2 surgeons will operate with all three diathermy settings. All other aspects of the abdominoplasty will proceed as per usual practice. The control will be monopolar coagulation diathermy with power setting of 35W .

Sponsors

Dr Amira Sanki
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

All adult patients presenting to the Surgeons involved who are undergoing abdominoplasty and provide informed consent to partake

Exclusion criteria

Those who do not consent to participate.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026