ClinicalTrials.Veeva

Menu

Topical Insulin for Postoperative Wound Healing

Cairo University (CU) logo

Cairo University (CU)

Status

Active, not recruiting

Conditions

Insulin Resistance, Diabetes
Wound Complication

Treatments

Drug: Insulin
Drug: Povidone-Iodine

Study type

Interventional

Funder types

Other

Identifiers

NCT06400082
16-4-2023

Details and patient eligibility

About

This study aimed to investigate the potential effect of applying topical insulin therapy on the management and healing of postoperative wounds in patients known with type 2 diabetes mellitus (T2DM) and in a parallel group without diabetes. Investigators also studied the effect of topical insulin therapy on the expression of e-cadherin and Ki67, as markers for cellular proliferation and wound repair. The levels of IL-6 and the H2O2-induced DNA damage product, 8-hydroxy-2'-deoxyguanosine (8-OHdG), were assessed as markers for inflammation and oxidative stress. Finally, histomorphological assessment of skin biopsies was also carried out.

Full description

The study participants will be recruited from general surgery department ,all patients with elective surgical procedure who will be admitted at the department for at least one week as it is the minimal duration of postoperative wound healing and the study will be conducted according to the regulations of ethical committee of clinical studies in the Faculty of Medicine, Cairo University

Enrollment

74 patients

Sex

All

Ages

40 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Both males and females
  • 40-60 years old
  • diagnosed with type 2 DM (for the diabetic trial)
  • For the diabetic trial: glycosylated hemoglobin (HBA1c) ≤7.5 %
  • haemoglobin (Hb) ≥ 12 g/dl
  • Patients who had a full thickness post-operative wound of ≥10 cm

Exclusion criteria

  • Those with known history of immunodeficiency, keloid formation, or hyperkeratotic skin lesion.
  • Patients who had hypersensitivity to insulin,
  • Patients with severe infection,
  • Patients with any severe organ dysfunction
  • Patients who were admitted to ICU

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

74 participants in 2 patient groups

Povidone iodine 10%
Active Comparator group
Treatment:
Drug: Povidone-Iodine
Topical insulin
Experimental group
Treatment:
Drug: Insulin

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems