Clinical Trials Directory

Trials / Terminated

TerminatedNCT00787176

The Association Between Fluid Administration, Oxytocin Administration, and Fetal Heart Rate Changes

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
251 (actual)
Sponsor
Northwestern University · Academic / Other
Sex
Female
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

Fetal heart rate patterns are an important parameter in the diagnosis of non-reassuring fetal status. Combined-spinal epidural analgesia is a method of initiating labor analgesia used by approximately 90% of the parturients at Prentice Women's Hospital. Optimizing the variables which could affect fetal heart rate patterns at the time of initiation of analgesia, such as fluid administration and oxytocin management, could help us provide better care for our patients and their fetuses. Hypotheses: The combination of fluid administration and lower doses of oxytocin administration will have fewer adverse fetal heart rate changes in the first 60 minutes following initiation of labor analgesia.

Detailed description

After obtaining informed, written consent, candidates were randomized to one of four groups at the time of request for labor analgesia. All subjects received a maintenance infusion of Lactated Ringers(LR). For candidates in Groups A or B, an intravenous bolus of 1000 mL of LR was initiated. Candidates in Groups C and D did not receive any additional fluid. If randomized to group A or C, the oxytocin management was continued as per the normal active management of labor protocal (AMOL). If randomized to groups B or D, the dose of oxytocin that was being administered was halved and not increased until 60 minutes after the initiation of epidural analgesia. Fetal heart rate monitoring and frequency of uterine contractions were recorded by external tocodynamometry.

Conditions

Interventions

TypeNameDescription
DRUGGroup A Intravenous bolus of 1000 ml lactated ringers solutionAn intravenous bolus of 1000 mL Lactated Ringers initiated when the patient was positioned for epidural placement. Oxytocin management continued as per protocol.
DRUGGroup B Intravenous bolus bolus 1000 ml lactated ringers solution oxytocin decrease to 1/2 current rateAn intravenous bolus of 1000 mL Lactated Ringers. The dose of oxytocin being administered at time of epidural placement will be halved and not increased for 60 minutes until after placement.
DRUGGroup C 125 mL/hr of lactated ringersThe maintenance infusion of 125 mL/hr of Lactated Ringers will be given with no additional fluid bolus. Oxytocin management continued per protocol.
DRUGGroup D 125 mL/hr lactated ringers oxytocin decreased to 1/2 current rateThe maintenance infusion of 125 mL/hr of Lactated Ringers was given with no additional fluid bolus. The dose of oxytocin being administered at time of epidural placement will be halved and not increased for 60 minutes until after placement.

Timeline

Start date
2007-09-01
Primary completion
2012-07-01
Completion
2012-07-01
First posted
2008-11-07
Last updated
2022-01-13
Results posted
2022-01-13

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00787176. Inclusion in this directory is not an endorsement.