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Not yet recruitingNCT07476261Updated Mar 17, 2026

Incidence of Ssi After c.s

An observational study in Site Infection, sponsored by Assiut University. Not yet recruiting at 1 site in Egypt. Open to female participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2026-03-17.

Sponsored by Assiut University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
105
Ages
18 Years to 45 Years
Sex
Female
01

Study summary

aim of the work is to evaluate adherence to preoperative , intraoperative, and postoperative infection preventive measures during cesarean section and to assess it s impact on the incidence of surgical site infection and maternal well-being during 30 days postoperative peroid.

Read the detailed description

Cesarean Section is one of the most commonly performed obstetric surgical procedures worldwide. Despite its importance in reducing maternal and fetal complications, it is associated with several postoperative complications, the most important of which is Surgical Site Infection. Surgical site infection after cesarean section can lead to increased maternal morbidity, prolonged hospital stay, and higher healthcare costs. Therefore, evaluating the incidence of surgical site infection and assessing adherence to preventive measures are essential for improving the quality of obstetric care. This study aims to determine the incidence of surgical site infection after cesarean section and to assess compliance with infection prevention strategies.

02

Conditions studied

  • Site Infection
03

In context

Lead sponsor

Assiut University is the lead sponsor of 4,901 studies on the registry; 2,098 are open to participants now.

Of its 13 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Sampling method
Non-probability sample

Study population

The study population will include all women undergoing Cesarean Section at El-Mabarra Health Insurance Hospital during the study period. Eligible participants will be followed for 30 days after delivery to detect the occurrence of Surgical Site Infection. Women who meet the inclusion criteria and agree to participate in the study will be enrolled consecutively until the required sample size is reached.

Inclusion criteria

  • All women who underwent cesarean section during the study period

Exclusion criteria

Exclusion Criteria:

  • Patients who are lost to follow-up before completion of the 30-day postoperative assessment.

Patients with immunocompromised conditions, such as:

Chronic corticosteroid therapy. Immunosuppressive treatment. Known HIV infection with severe immunosuppression .

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
105 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. incidence of surgical site infection after cesarean section

    superficial or deep surgical site infection

    Time frame: Baseline

07

Study locations

1 site
  • El Mabarra Health Insurance Hospital.
    Asyut, Egypt
08

References and documents

Publications

  • Naeem A, et al. Incidence of surgical site infection after cesarean section. 2025.
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 17, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07476261
Lead sponsor
Assiut University
Responsible party
mona magdy helmy (resident doctor, Assiut University) — Principal investigator
First posted
Mar 17, 2026
Start date
May 1, 2026 (estimated)
Primary completion
May 1, 2027 (estimated)
Completion
Aug 1, 2027 (estimated)
Last update
Mar 17, 2026

Study contacts

mona madgy
Contact
mona.helmy1997@gmail.com
01145421696

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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