Current partner codePEPTIDESDE
NCT03939806·Not applicable·OBSERVATIONAL

Effects of Oxytocin and Carbetocin on Renal System in Cesarean Sections

Status

Unknown

Phase

Not applicable

Enrollment

100

Locations

1

Results

Not posted

Publications

2

Study summary

What the protocol is testing.

The aim of this study is to evaluate the renal outcome of patients undergoing elective C/S where oxytocin or carbetocin is used for postpartum hemorrhage prophylaxis.

Interventions

Treatment arms and agents.

DRUG

Oxytocin

To be given to Oxytocin group following the clamping of the umbilical cord

DRUG

Carbetocin

To be given to Carbetocin group following the clamping of the umbilical cord

Timeline

From registration to results.

  1. First posted

    May 7, 2019

  2. Study start

    May 2019

  3. Primary completion

    Jun 2019

  4. Study completion

    Jun 2019

  5. Results posted

    Not reported

  6. Registry updated

    May 13, 2019

Outcomes

What the study measures.

Primary outcomes

Urine volume

Time frame · Intraoperative period

Total amount of intraoperative urine output in milliliters

Urinary sodium

Time frame · Preoperative, Postoperative 2nd, 4th, 24th hours

The change in urinary sodium content (milligrams) compared to the preoperative period

Blood sodium

Time frame · Preoperative, Postoperative 2nd, 4th, 24th hours

The change in blood sodium content (milligrams) compared to the preoperative period

Secondary outcomes

Blood osmolality

Time frame · Preoperative, Postoperative 2nd, 4th, 24th hours

The change in blood osmolality compared to the preoperative period

Blood loss

Time frame · Intraoperative period

The total volume of intraoperative blood loss

Need for additional uterotonics

Time frame · Starting from the preoperative period, ending at the 24th postoperative hour

Total dose (milligrams) of additional uterotonics administered

Blood transfusion

Time frame · Starting from the clamping of the umbilical cord, ending at the 24th postoperative hour

Total volume (milliliters) of blood transfused

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
65 Years
Sex
FEMALE
Healthy volunteers
No

Inclusion Criteria: * Term (\>37 weeks of gestation) uncomplicated pregnant women undergoing elective cesarean section Exclusion Criteria: * Patients refusing to participate in the study * Complicated pregnancies * Patients with risk factors for postpartum hemorrhage * Contraindications for oxytocin or carbetocin usage * Patients with known renal diseases * Preterm births (\<37 weeks of gestation)

Study locations

1 registered sites.

Turkey (Türkiye). Showing up to 24 locations stored in the fast local snapshot.

Ufuk University Faculty of Medicine Hospital

Ankara, Balgat, Turkey (Türkiye)

Related trials

More studies on Carbetocin.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.