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A RANDOMIZED CONTROLLED STUDY OF HONEY AND IODINE PASTES IN WOUND HEALING AFTER CAESAREAN SECTION

A randomized controlled study of honey and iodine pastes in wound healing after caesarean section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202504494184668
Enrollment
120
Registered
2025-04-07
Start date
2025-02-28
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

wound healing after caesarean section

Interventions

Honey
Iodine paste
Negative Control

Sponsors

Federal University of Health Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: a. All booked and stable pregnant women who are admitted for elective caesarean sections b. Term pregnancy c. Informed consent to participate in the study after counselling d. Low transverse abdominal incisions will be recruited.

Exclusion criteria

Exclusion criteria: a. Pregnant women with medical conditions such as Diabetes mellitus, chronic renal diseases, autoimmune disease, collagen vascular diseases, etc, that may interfere with the healing process. b. Women with untreated anaemia in pregnancy c. Refuse consent d. Women planned for elective caesarean section but ended up with vaginal delivery e. consumption of drugs affecting wound healing, such as corticosteroids, anticoagulants, immunosuppressants and chemotherapy. f. Uncontrolled medical conditions in pregnancy such as Diabetes mellitus

Design outcomes

Primary

MeasureTime frame
Rate of wound healing using REEDA Score. The score will be used to assess the Redness, Edema, Ecchymosis, Discharge and Apposition. The total score will be interpreted as - Healed = 0; moderately healed = 1 to 5; mildly healed = 6 to 10; not healed = 11 to 15. The participant will be studied at a 7-day interval until the wound is healed and the REEDA score is 0.

Secondary

MeasureTime frame
Rate of SSI. The diagnosis of the surgical site infection is clinical, and the rate will be determined by the number of infected wounds by 40 at the time of wound inspection.;Infective microorganism isolated from the SSI. A wound swab will be taken of the infected wound and sent for mciroscopy, culture, and sensitivity testing. The infective microorganism will be isolated in the laboratory. ;antibiotic sensitivity. For each of the infective microorganism isolated from the SSI, an antibiogram will be done to determine the antibiotic sensitivity

Countries

Nigeria

Contacts

Public ContactAisha Kyari

Co researcher and Senior Registrar at the University of Maiduguri Teaching Hospital

ayeshababakyari@gmail.com+2348032838148

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026