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Evaluation the effect of amniotic membrane graft on wound healing process and decrease complications in patient who undergone anal fistulatomy

Evaluation the effect of amniotic membrane graft on wound healing process and decrease complications in patient who undergone anal fistulatomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201310219936N6
Enrollment
85
Registered
2013-11-15
Start date
2012-07-10
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Anal fistula. Anal fistula

Interventions

Intervention 1: In group B: Amniotic membrane is not the only place marsupialization thread Monocryl (0-4). Intervention 2: In group A : Amniotic membrane graft group patients using 0-4 suture is Mon
Treatment - Surgery
In group B: Amniotic membrane is not the only place marsupialization thread Monocryl (0-4).
In group A : Amniotic membrane graft group patients using 0-4 suture is Monocryl (amniotic membrane on the bottom layer to the edges of the fistula tract located Monocryl thread is fixed)

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 18-65 years old; low type fistula; first time to be operated. Exclusion: history of TB and ; history of previous fistula operation; high type fistula; immunosuppression; procitis; radiotherapy; complex fistula; stool or gas incontinency and egg allergy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Post operation complication. Timepoint: 1, 3, 7, 21, 28th days of post operation. Method of measurement: Evaluation of score of pain after surgery in both groups with visual analog scale (VAS).

Secondary

MeasureTime frame
Discharge. Timepoint: 1, 3, 7, 21 and 28th days of post operation. Method of measurement: Subjectively.;Itching. Timepoint: 1, 3, 7, 21 and 28th days of post operation. Method of measurement: Subjectively no variable.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Alireza Safarpour

Colorectal Research Center, Shiraz university of medical sciences

fsafarpour@yahoo.com+98 71 1230 6972

Outcome results

None listed

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