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Evaluation of the Relationship Between Obstetric Comorbidity Index and Obstetric Quality of Recovery Score

P

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

Status

Completed

Conditions

Cesarean Section Complications
Quality of Life
Obstetric Complication
Obstetric Anesthesia Problems
Comorbidities and Coexisting Conditions

Treatments

Other: Obstetric Quality of recovery score

Study type

Observational

Funder types

Other

Identifiers

NCT05704179
23052022162

Details and patient eligibility

About

The goal of this prospective observational study is to learn about the correlation between obstetric comorbidity index and obstetric quality of recovery score in pregnant patients who undergo cesarean section. The main question aims to answer are:

  • Are there a correlation between the obstetric comorbidity index and the obstetric quality of recovery score? Can we predict the postoperative quality of recovery by calculating the obstetric comorbidity index before delivery?
  • What is the relationship between these scores with the type of anaesthesia given? Participants will answer an 11-question assessment scale to evaluate their recovery of quality in the postpartum period.

Full description

After the approval of the ethics committee and the written informed consent of the patients, the patients who are meeting the criteria of inclusion will be included in the study. The demographic data, type of anaesthesia, intraoperative haemorrhage, length of hospital stay and intensive care unit stay(if applicable), the urgency category of the cesarean section, and complications will be recorded. patients will be evaluated with obstetric quality of recovery assessment score on postpartum 1st and 2nd days

Enrollment

214 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Pregnant women who are admitted for Cesarean section > 18 years old
  • Speaking Turkish or English
  • Agreeing to participate in the study

Exclusion criteria

  • Pregnant women < 18 years old
  • Can not speak Turkish or English
  • Not agreeing to participate in the study

Trial design

214 participants in 1 patient group

Patients who undergo cesarean section
Description:
Obstetric comorbidity index will be calculated for all patients, obstetric quality of recovery score will be evaluated in postpartum period( on the first and second day postpartum)
Treatment:
Other: Obstetric Quality of recovery score

Trial contacts and locations

1

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Central trial contact

Gaye Şensöz Çelik; Fethi Gültop

Data sourced from clinicaltrials.gov

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