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Are Sutures Required in Total Abdominal Hysterectomy? A Randomised Control Trial

S

Southern Health

Status and phase

Unknown
Phase 1

Conditions

Total Abdominal Hysterectomy

Treatments

Procedure: Performing abdominal hysterectomy using gyrus electrocoagulation forceps

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT00484835
Electrocoag Forceps in TAH

Details and patient eligibility

About

The Hypothesis of this study is that performing total abdominal hysterectomy using the newer electrocoagulation forceps, specifically, the gyrus open seal forceps, curved, compared to the traditional clamp & suture technique will result in reduction of operating time, intra-operative blood loss, post-operative pain.

Full description

Patients booked for total abdominal hysterectomy in Southern Health will be offered participation in the trial, and randomised to two groups: one group undergoing the procedure with the gyrus forceps & the other group with the traditional clamp & suture method. Each patient will receive detailed information regarding the study both in document form as well as verbally by the Gynaecology doctors in the pre-admission clinic prior to obtaining consent.

The researcher will collect relevant data including age of patient, medical & surgical history and data relating to both the primary & secondary outcome measures, which include length of operation, intra-operative blood loss,post-operative pain measures as well as length of hospital stay & cost.

A qualified statistician will perform power calculations and analyse the data collected, looking at the outcome measures mentioned above.

Electrical surgery has been used extensively in surgery, especially in laparoscopic surgery, and the use of these newer electrocoagulation forceps that can simultaneously haemostatically seal & cut tissue is again well established in laparoscopic surgery but only more recently introduced to open surgical procedures. To date, except for 1 pilot study, there are no randomised control trials that confirm the proposed benefits of these newer device in abdominal hysterectomy.

Enrollment

60 estimated patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Any patient already on waitlist in Southern Health for abdominal hysterectomy with suspected benign pathology

Exclusion criteria

  • Patients without consent and/or with suspected malignant pathology

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

3

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Central trial contact

Marziya Kadir, MBBS; Jason Tan, MBBS, MRANZCG

Data sourced from clinicaltrials.gov

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