NCT07406607 The Effect of Presence of Father in the Operating Room on Quality of Recovery of the Parturient
| NCT ID | NCT07406607 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Karamanoğlu Mehmetbey University |
| Condition | Caesarean Section |
| Study Type | INTERVENTIONAL |
| Enrollment | 110 participants |
| Start Date | 2026-02-19 |
| Primary Completion | 2026-06-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 110 participants in total. It began in 2026-02-19 with a primary completion date of 2026-06-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The presence of a partner to support the mother during cesarean and vaginal deliveries is a well-established practice in most countries worldwide. It is evident that allowing the partner into the operating room during a cesarean section provides psychosocial benefits for both the mother and the partner. This study aims to investigate the effect of the presence of partner in the operating room on quality of recovery of parturients at the postoperative period.
Eligibility Criteria
Inclusion Criteria: * Patients scheduled for an elective cesarean section. * Patients and their partners must be literate in Turkish (able to read and write) to accurately complete the study questionnaires * Patients and their partners must be willing and able to provide written informed consent * Healthy pregnant women with no additional chronic or systemic diseases (comorbidities) * The operating surgeon must have at least 5 years of professional experience and no chronic health conditions. Exclusion Criteria: * Patients undergoing emergency cesarean sections. * Patients with any known chronic or systemic additional diseases * Surgeons with any known chronic or systemic diseases. * Individuals unable to read or understand the Turkish questionnaires (implied by the literacy requirement). * Patients with American Society of Anesthesiologists (ASA) classification of 3 or more * Patients with history of chronic pain, chronic use of analgesic drugs, or history of opioid or intravenous drug abuse * Patients who have refused spinal anesthesia, or those in whom it is contraindicated. * Pregnancy with preeclampsia or eclampsia * Pregnancy with gestational diabetes mellitus or diabetes mellitus
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07406607 clinical trial?
This trial is open to female participants only, aged 18 Years or older, up to 45 Years, studying Caesarean Section. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07406607 currently recruiting?
Yes, NCT07406607 is actively recruiting participants. Contact the research team at gamzesavci42@gmail.com for enrollment information.
Where is the NCT07406607 trial being conducted?
This trial is being conducted at Karaman, Turkey (Türkiye).
Who is sponsoring the NCT07406607 clinical trial?
NCT07406607 is sponsored by Karamanoğlu Mehmetbey University. The trial plans to enroll 110 participants.