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NCT03269188 Clinical Trial

Incidence and Associated Factors of Persistent Postoperative Incision Scar Pain Following C/s in Mulago Hospital

Chronic Pain Clinical Trial

— PPOPinC/S  

Official title:
Incidence and Associated Factors of Persistent Postoperative Incision Scar Pain Following C/s in Mulago Hospital

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03269188
Other study ID # Persistent pain in C/S
Secondary ID
Status Completed
Phase N/A
First received August 30, 2017
Last updated August 30, 2017
Start date July 6, 2016
Est. completion date October 27, 2016

Study information
Verified date August 2017
Source Makerere University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

prospective cohort study of women who underwent caesarean section in mulago hospital. followed up for 2 months and assessed for development of persistent post operative pain at the incision site and its effect on quality of life. incidence of persistent postoperative pain and associated factors determined.

Description:

prospective cohort study of 277 women who underwent caesarean section in mulago hospital. demographic, medical history, intraoperative, postoperative details, and perioperative levels of pain collected. followed up by telephone interviews for 2 months and assessed for development of persistent post operative pain at the incision site and its effect on quality of life. incidence of persistent postoperative pain and associated factors determined.

Recruitment information / eligibility
Status Completed
Enrollment 277
Est. completion date October 27, 2016
Est. primary completion date October 10, 2016
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- ASA I, II, and III.

- patient who has given informed consent.

Exclusion Criteria:

- patients who have no telephone contact

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Makerere University

Outcome
Type Measure Description Time frame Safety issue
Primary persistent postoperative pain at caesarean section incision scar site. participant report pain at site of caesarean section incision site scar at 2 months after caesarean section. 2 months.
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