CClinicalTrials.gg
Status unknownNCT03007706Updated Jan 4, 2017

Role of Skin Cleansing and Prophylactic Antibiotic in Preventing Infectious Morbidity After Cesarean Section Delivery

An observational study in Postpartum Infectious Morbidity in Cesarean Section Delivery, sponsored by Raghda Gamal Mohamed. Status unknown. Open to female participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-01-04.

Sponsored by Raghda Gamal Mohamed · Observational

The sponsor has not verified this record recently (last verified Dec 2016), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
200
Ages
18 Years to 45 Years
Sex
Female
01

Study summary

This study aims to determine the effectiveness of skin cleansing and prophylactic antibiotics given to women undergoing a cesarean section for reducing the incidence of postpartum infectious morbidity and to assess potential maternal adverse effects and any impact on the infant.

02

Conditions studied

  • Postpartum Infectious Morbidity in Cesarean Section Delivery
03

In context

Communicable Diseases

4,452 studies on the registry are indexed under Communicable Diseases; 521 are open to participants now.

This study's planned enrollment of 200 is below the median of 244 across 1,499 observational studies indexed under Communicable Diseases.

Browse Communicable Diseases studies →

Lead sponsor

This is the only study on the registry with Raghda Gamal Mohamed as lead sponsor.

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

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

women undergo cesarean section delivery whether elective or emergency

Inclusion criteria

  1. Women undergoing cesarean delivery, both elective and non-elective.
  2. Rupture of membranes and labor contractions will be allowed.

Exclusion criteria

Exclusion Criteria:

  1. Unknown outcome from the patient.
  2. Refusing to participate in the study from the admission conse
  3. Allergy to antibiotics.
  4. Any visible infection.
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
200 participants (estimated)
Target follow-up
2 Weeks
Patient registry
Yes

Interventions

  • ProcedureWomen undergo cesarean section delivery
06

What researchers measure

Primary outcomes

  1. role of skin cleansing and prophylactic antibiotics given to women undergoing a cesarean section for reducing the incidence of postpartum infectious morbidity

    Time frame: 2 weeks following cesarean section

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 4, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03007706
Lead sponsor
Raghda Gamal Mohamed
Responsible party
Raghda Gamal Mohamed (Minia university, Minia Maternity University Hospital) — Sponsor-investigator
First posted
Jan 2, 2017
Start date
Jan 2017
Primary completion
Jun 2017 (estimated)
Completion
Oct 2017 (estimated)
Last update
Jan 4, 2017
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2016. You cannot join it, but the record below documents what was studied.

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