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Clinical Trials/NCT07053930
NCT07053930CompletedNot Applicable

To Compare the Mean Duration of Third Stage of Labour Between Intraumbilical and Intravenous Oxytocin.

RESnTEC, Institute of Research1 site in 1 country100 target enrollmentStarted: October 1, 2024Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
100
Locations
1
Primary Endpoint
Duration of the third stage labour

Study Overview

Brief Summary

There is always a debate for choosing the best method for management of the third stage of labour (TSL) in the general practice for reducing the duration of TSL. Although intravenous oxytocin is more extensively used in general practice for managing TSL than intraumbilical, it still needs to be properly investigated among local populations and in local settings.

Detailed Description

The findings of this study could identify the better route of oxytocin injection that could guide clinicians and health providers to opt for the better route in their routine practice for the management of TSL in order to reduce the morbidity and mortality of the patients, especially for developing countries like Pakistan, where most of the deliveries are conducted at peripheral or rural centers by a nurse, midwife, or a trained dai.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Females aged 18-40 years
  • With spontaneous vaginal delivery
  • Singleton pregnancy
  • Gestational age >37 weeks
  • Parity l-5
  • Any gravidity

Exclusion Criteria

  • Females with intrauterine fetal death
  • Malpresentation
  • Multiple pregnancy
  • Polyhydramnios
  • Premature rupture of membranes
  • Medical disorders and hypertensive disorders of pregnancy

Arms & Interventions

Intraumbilical oxytocin group

Experimental

Patients were given 10 U of intraumbilical oxytocin, diluted in 10 mL of normal saline.

Intervention: Intraumbilical oxytocin (Drug)

Intravenous oxytocin group

Experimental

Patients received 20 U of intravenous oxytocin diluted in 500 mL of normal saline.

Intervention: Intravenous oxytocin (Drug)

Outcomes

Primary Outcomes

Duration of the third stage labour

Time Frame: 30 minutes

The duration of the third stage labour was measured from the completed delivery of the newborn until the completed delivery of the placenta.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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