NCT02810639

Completed

Pain Prevalence After Cesarean Section in Siriraj Hospital

Mahidol University Source

Other study identifiers

Sponsor study identifier

816/2554(EC3)

Study Type

observational

Actual enrollment (reported)

297

Locations

1 country

Sites

1

Timeline

Study Start

March 2013

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

June 2013

Actual (reported)

Study Completion

June 2013

Actual (reported)

Brief Summary

Spinal morphine has been widely provided for acute postoperative analgesia. However, the analgesic effect of spinal morphine usually last 12-24 hours. Therefore the investigators are interested in the pain characteristics during the 2nd postoperative day. The investigators will also explore the regimens for pain therapy in our hospital.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 297 participants
Study completion date: June 2013
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
March 2013
Date type not reported
This date has not been verified as actual or estimated.
Primary Completion
June 2013
Actual (reported)
Study Completion
June 2013
Actual (reported)
First Submitted
June 17, 2016
Actual (reported)
First Posted
June 23, 2016
Actual (reported)

Last Updated: June 23, 2016
Status Verified: June 2016
Last Update Submitted: June 22, 2016

Conditions

Pain, Postoperative

Keywords

pain

Outcome Measures

Primary Outcomes (1)

Number of patients who have moderate to severe pain after Cesarean section
Number of patients who have moderate to severe pain after Cesarean section
24-48 hours

Eligibility Criteria

Age18 Years+

Sexfemale

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

Patients undergoing Cesarean section

You may qualify if:

Patients undergoing Cesarean section

You may not qualify if:

Sponsors & Collaborators

Mahidol University
Otherlead

Study Sites (1)

Sirilak Suksompong

Bangkok, 10700, Thailand

MeSH Terms

Conditions

Pain, PostoperativePain

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsNeurologic ManifestationsSigns and Symptoms

Study Officials

Sirilak Suksompong, MD
Mahidol University
PRINCIPAL INVESTIGATOR

Enrollment

297 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: COHORT
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Associate Professor

Study Record Dates

First Submitted

June 17, 2016

First Posted

June 23, 2016

Study Start

March 2013

Date type not reported

This date has not been verified as actual or estimated.

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NCT01465191

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Phase 4Completed

NCT01898052

The Efficacy of Periarticular Single Drug Compared With Multimodal Drug Injection in Controlling Pain After TKA

Phase 4Completed

NCT03549221

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Phase 2Unknown

History of drug addict

Contact the study team to confirm eligibility.

Primary Completion

June 2013

Actual (reported)

Study Completion

June 2013

Actual (reported)

Last Updated

June 23, 2016

Record last verified: 2016-06

Data Sharing

IPD Sharing: Will not share

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT02810639
Data provider: ClinicalTrials.gov
Source updated: 2016-06-23
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:27:44 UTC

Locations

TH(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

Primary Completion

Study Completion

First Submitted

First Posted

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

Data Sharing

Source record

Locations