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Enrolling by invitation NCT07641751

Effect of Husband Attendance on Anesthesia Performance and Maternal-Neonatal Outcomes During Elective Cesarean Section Under Spinal Anesthesia

No phase Interventional Husband Attendance Maternal-Neonatal Outcomes

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Husbands will be allowed to attend the cesarean section procedure, providing emotional support to their partners., Husbands will not be permitted to attend the cesarean section procedure.
Who it may be relevant to
Registry conditions: Husband Attendance, Maternal-Neonatal Outcomes. Basic parameters: No limits · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effect of Husband Attendance on Anesthesia Performance and Maternal-Neonatal Outcomes During Elective Cesarean Section Under Spinal Anesthesia: A Randomized Controlled Trial

Overview

Family-centered perinatal care has become an integral component of modern obstetric practice, emphasizing emotional support and shared parental experiences during childbirth. The presence of an additional individual in the operating room may influence workflow dynamics, potentially introducing distractions or compromising adherence to sterile protocols. These factors could theoretically affect anesthesia administration, surgical timing, and perioperative safety. Conversely, emotional support from the husband may reduce maternal anxiety, improve overall experience, and indirectly influence physiological responses during surgery.

Interventions

  • Behavioral Husbands will be allowed to attend the cesarean section procedure, providing emotional support to their partners.
    Husbands will be allowed to attend the cesarean section procedure, providing emotional support to their partners.
  • Behavioral Husbands will not be permitted to attend the cesarean section procedure
    Husbands will not be permitted to attend the cesarean section procedure

Primary outcome measures

  • Anesthesia Administration [Time frame: intraoperative period]
  • Surgical Delays [Time frame: intraoperative period]
  • Complications [Time frame: intraoperative period]
  • Sterility and Infection Control [Time frame: perioperative period]
Secondary outcome measures (2)
  • Patient Satisfaction [Time frame: immediately after the procedure]
  • Neonatal Outcomes [Time frame: 1 and 5 minutes after neonatal delivery]

Eligibility criteria

Inclusion criteria

  • Eligible participants will include primiparous and multiparous women scheduled for elective cesarean section under spinal anesthesia, performed by experienced anesthesiologists.

Exclusion criteria

  • contraindication of spinal anesthesia

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Health services research

Study locations

Egypt · 1 center
  • medical research institute , Alexandrria university — Alexandria

Publications

  • Bryanton J, Gagnon AJ, Johnston C, Hatem M. Predictors of women's perceptions of the childbirth experience. J Obstet Gynecol Neonatal Nurs. 2008 Jan-Feb;37(1):24-34. doi: 10.1111/j.1552-6909.2007.00203.x. PMID 18226154
  • Bohren MA, Hofmeyr GJ, Sakala C, Fukuzawa RK, Cuthbert A. Continuous support for women during childbirth. Cochrane Database Syst Rev. 2017 Jul 6;7(7):CD003766. doi: 10.1002/14651858.CD003766.pub6. PMID 28681500

Identifiers

NCT: NCT07641751 · Husband Attendance in CS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗