Skip to main content
Clinical Trials/CTRI/2018/09/015665
CTRI/2018/09/015665CompletedNot Applicable

"Effectiveness of early ambulation on post operative recovery among primiparous post caesarean mothers"

Self funded1 site in 1 country124 target enrollmentStarted: September 17, 2018Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
124
Locations
1
Primary Endpoint
Post operative recovery

Study Overview

Brief Summary

I did a study of effectiveness of early ambulation on post operative recovery. For that i have used randomized control group. My sample size was 124, 62 in each interventional and control group. In intervention group i have provided ambulation after 6 hours of surgery as a intervention. I have ambulted thrice in day for 1st 5 post operative days. After every 24 hours i have assessed post operative recovery by structured observational schedule. Before ambulation i assesed pain by numeric pain rating scale. In control group early ambulation was not provided instead hospital protocol of ambulation was followed for them and same assessment sheet was be used to assess the post operative recovery.

Study Design

Study Type
Interventional
Allocation
Computer generated randomization
Masking
Investigator Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 45.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • mothers who have undergone caesarean section for the first time, those who have undergone under spinal anesthesia and those who can understand verbal communication.

Exclusion Criteria

  • mothers those who have other medical and gynecological complication, mother who have undergone through general anesthesia, mother who have cardiac problem, magnesium sulfate therapy, immediate postpartum complications and those have doctors order for strict bed-rest.

Outcomes

Primary Outcomes

Post operative recovery

Time Frame: Post operative recovery

Secondary Outcomes

  • Early ambulation after surgery(After 6 hours of surgery)

Investigators

Sponsor
Self funded
Sponsor Class
Research institution and hospital

Study Sites (1)

Loading locations...

Similar Trials