NCT05181358

Brief Summary

The question remains whether the patients in whom USG-guided regional anesthesia and analgesia techniques are applied have a better recovery score than subarachnoid morphine administration, which is considered the gold standard. The primary aim of this study is to evaluate the quality of recovery score using the Obstetric Recovery Quality Score-ObsQoR-10 questionnaire experienced by the patients who underwent elective cesarean section and compare the results of different regional anesthesia techniques with subarachnoid morphine.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
180

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2022

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 19, 2021

Completed
18 days until next milestone

First Posted

Study publicly available on registry

January 6, 2022

Completed
18 days until next milestone

Study Start

First participant enrolled

January 24, 2022

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 26, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 26, 2022

Completed
Last Updated

January 26, 2023

Status Verified

January 1, 2023

Enrollment Period

11 months

First QC Date

December 19, 2021

Last Update Submit

January 23, 2023

Conditions

Quality of RecoveryCesarean Section

Keywords

Quality of recoveryObsQoR-10regional analgesia

Outcome Measures

Primary Outcomes (1)

  • Obstetric Quality of Recovery

    Obstetric Quality of Recovery-10 (ObsQoR-10©) Scoring Tool

    The first 24 hours postoperatively

Eligibility Criteria

Age18 Years - 47 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailsonly the patients who underwent elective cesarean section will be recruited
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Term obstetric patients who underwent elective cesarean section under spinal anesthesia

You may qualify if:

  • Term obstetric patients aged 18-47 years who underwent elective cesarean section under spinal anesthesia and applied regional anesthesia techniques such as lateral TAP, posterior-TAP, QL, ESP, and TFD blocks or subarachnoid morphine.

You may not qualify if:

  • Patients with psychiatric disorders
  • Patients requiring emergency cesarean section.
  • Patients with additional obstetric pathology (such as placenta previa, preeclampsia, DM)
  • The need for intensive care in the mother or newborn at the end of the birth.
  • Patients who have undergone general anesthesia.
  • Preterm pregnants

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Betul Kozanhan

Konya, 42005, Turkey (Türkiye)

Location

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Ass.Prof.

Study Record Dates

First Submitted

December 19, 2021

First Posted

January 6, 2022

Study Start

January 24, 2022

Primary Completion

December 26, 2022

Study Completion

December 26, 2022

Last Updated

January 26, 2023

Record last verified: 2023-01

Locations

TU(1)