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Efficacy and Safety of Purified Starch for Adhesion Prevention in Colorectal Surgery

T

Taipei Medical University

Status

Completed

Conditions

Adhesions Abdominal

Treatments

Procedure: Second surgery

Study type

Observational

Funder types

Other

Identifiers

NCT05580484
N202109018

Details and patient eligibility

About

Intra-abdominal adhesion occurs in up to 90% of patients after abdominal surgery. Many patient will undergo a second surgery for temporary stoma closure, therefore these ostomy closure operations can give an opportunity to evaluate adhesion caused by previous operations. This study was conducted to use second surgery to investigate the anti-adhesion effect of purified starch among patients who underwent colorectal surgery.

Full description

Data was analyzed from the medical records of patients who underwent a second surgery after colectomy between January 2020 and April 2022. Patient were allocated to either the purified starch group and control group. Since January 2020, adhesion scores have been registered in operation note when patients undergo a second colorectal surgery. The primary outcomes in this study were adhesion severity and adhesion area. The secondary outcomes were operation time, blood loss, and postopera-tive complications.

Enrollment

83 patients

Sex

All

Ages

20 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who underwent a second surgery after colorectal resection between January 2020 and April 2022 were enrolled into this study.

Exclusion criteria

  • Patients who underwent a second surgery less than 1 month after the first colorectal resection or who developed peritoneum carcinomatosis in the second surgery and patients younger than 20 years were excluded.

Trial design

83 participants in 1 patient group

Purified starch/Control group
Description:
Patients who were willing to receive purified starch at their own expense during this first surgery were included in the purified starch group, and patients who did not re-ceive purified starch or other anti-adhesion products were included in the control group.
Treatment:
Procedure: Second surgery

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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