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Pain Score and Opioid Consumption of Index and Previous Cesarean Delivery

NCT ID: NCT06178458

Last Updated: 2023-12-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

416 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-01-31

Study Completion Date

2025-12-31

Brief Summary

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Postoperative pain after cesarean delivery is common and affects on both mothers and children.

The goals of this retrospective observational study aim to predict pain score and opioid consumption of index cesarean delivery from pain score and opioid consumption of previous cesarean delivery.

Detailed Description

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The authors will review the medical records of recruited participants for demographic data as well as pain scores and opioid consumption of index cesarean delivery and previous cesarean delivery.

Conditions

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Pain Postoperative

Keywords

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cesarean delivery opioid consumption pain score

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Interventions

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No intervention

To collect data of pain score and opioid consumption of index and previous cesarean delivery

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients who had at least 2 cesarean deliveries
* Patients received spinal anesthesia and intrathecal morphine for cesarean delivery
* Patients received postoperative pain control as per standard protocol

Exclusion Criteria

* Patients with chronic pain prior to cesarean delivery
* Unable to give pain score
* Receiving general anesthesia for cesarean delivery
* Receiving postoperative pain control beyond the standard protocol
* Patients with multiple pregnancy, placenta abruption, placenta accrete, postpartum hemorrhage
* Patients with psychotic disorder
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Prince of Songkla University

OTHER

Sponsor Role lead

Responsible Party

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Sasikaan Nimmaanrat

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Boonsin Tangtrakulwanich, MD

Role: STUDY_CHAIR

Prince of Songkla University

Central Contacts

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Sasikaan Nimmaanrat, MD, MMed

Role: CONTACT

Phone: +66887907842

Email: [email protected]

Boonsin Tangtrakulwanich, MD

Role: CONTACT

Phone: +6674451149

Email: [email protected]

Other Identifiers

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66-348-8-1

Identifier Type: -

Identifier Source: org_study_id