Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT06380036 |
Other study ID # |
003AEstb/EC/01/2022 |
Secondary ID |
|
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
November 1, 2022 |
Est. completion date |
October 31, 2023 |
Study information
Verified date |
April 2024 |
Source |
Sheikh Zayed Medical College |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
A total of 80 patients with complex fistula in ano of both genders were included. All
patients in Group A underwent a loose seton technique. In group B, video-assisted fistula
tract surgery (VAAFTS) was performed.Twice daily Sitz baths, analgesics, and stool bulking
agents (bran) were used in follow-up care. Repeated examinations were carried out every four
weeks and recurrence was noted at the end of three months
Description:
Patients were equally allocated into two groups i.e. Group A & Group B by lottery method. In
both groups, the lower bowel was emptied by an enema about an hour before the operation. All
patients in Group A underwent the loose seton technique. The procedures were performed in the
operating room with the patient in the lithotomy position. Probing of the fistula tract was
done with a metallic malleable probe. The incision was given from the external opening of the
fistula to the anal verge, involving the skin, subcutaneous tissue, superficial part of the
external sphincter, and superficial part of the internal sphincter. After the insertion of
loose Seton, a non-absorbable suture was left loosely and kept in situ for three months.
In group B, video-assisted fistula tract surgery (VAAFTS) was performed. The patients were
positioned in the lithotomy position. The fistuloscope was then introduced into the external
opening and the procedure was performed, except for the closure of the internal opening,
which was performed with either a "figure of eight" suture or an advancement flap, rather
than using a stapler. The tracts were destroyed using electrocautery, the necrotic tissues
were removed, and the external openings were cored out and left open for drainage. The
patients were discharged the day following the procedure. Twice daily Sitz baths, analgesics,
and stool bulking agents (bran) were used in follow-up care. Repeated examinations were
carried out every four weeks and recurrence was noted at the end of three months. The
information (age, gender, duration of disease, BMI, diabetes mellitus, hypertension, place of
living, and recurrence) was collected through pre-designed Performa (Annexure I).