Clinical Trials Logo

Clinical Trial Summary

A case control trial Patients who meet the inclusion criteria were asked to participate in the study and a written consent was obtained from each patient after explaining thoroughly the nature and the scope of the study. Patients were divided into three equal groups: Group A: included 40 pregnant patients. They received two ml of normal saline intravenously as a placebo. Group B: included 40 pregnant patients. They received (20mg) hyoscine butylbromide (one ml HBB+ one ml saline) intravenously. Group C: included 40 pregnant patients .They received two ml (40 mg) hyoscine butylbromide intravenously (HBB).


Clinical Trial Description

A case control trial Patients who meet the inclusion criteria were asked to participate in the study and a written consent was obtained from each patient after explaining thoroughly the nature and the scope of the study. For each patient: 1. Complete history was taking to exclude allergy to hyoscine butylbromide, medical disorders with pregnancy (preeclampsia, diabetes mellitus, heart disease …etc.) and any contraindication for vaginal delivery. 2. General examination of the patients including (pulse, blood pressure, temperature). 3. Obstetric Abdominal examination including fetal lie, fetal presentation, head station and uterine contractions. 4. Vaginal examination including cervical dilatation, effacement and position, state of fetal membranes, presenting part, position of fetal head and pelvic adequacy. 5. Obstetric ultrasound to detect fetal gestational age, fetal birth weight amount of liquor, site of placental attachment and fetal heart rate. Patients were divided into three equal groups: Group A: included 40 pregnant patients. They received two ml of normal saline intravenously as a placebo. Group B: included 40 pregnant patients. They received (20mg) hyoscine butylbromide (one ml HBB+ one ml saline) intravenously. Group C: included 40 pregnant patients .They received two ml (40 mg) hyoscine butylbromide intravenously (HBB). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03055390
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase Phase 4
Start date February 11, 2017
Completion date February 3, 2022

See also
  Status Clinical Trial Phase
Completed NCT06126328 - Materna Prep Study Phase II Phase 2
Not yet recruiting NCT05501106 - Reducing Postpartum Hemorrhage After Vaginal Delivery N/A
Completed NCT05429580 - Prophylactic Tranexamic Acid Use After Vaginal Delivery N/A
Completed NCT05786911 - Postpartum Fatigue and Pain Versus Nutritional Status, With Epidural Analgesia
Completed NCT05371015 - Quadratus Lumborum Block Reduced Postpartum Uterine Pain After Virginal Childbirth N/A
Not yet recruiting NCT06202768 - Role of the Intrapartum Grobman Nomogram in the Indication of Attempted Vaginal Delivery After Cesarean Section
Terminated NCT04277962 - Estimating Blood Loss Using TritonTM in Vaginal Deliveries: A Validation Trial N/A
Terminated NCT04004845 - Labor Protocol Study
Not yet recruiting NCT05247073 - Mostafa Maged Four-stitch Technique in Closure the Episiotomy During Vaginal Delivery N/A
Recruiting NCT00407290 - The Impact of an Epidural Ropivacaine-Neostigmine Injection for Perineal Analgesia at the End of Labor. N/A
Terminated NCT01190163 - Open Label Comparative Trial of Dinoprostone Plus or Minus Oxytocin Versus Oxytocin Alone in Cervical Ripening for Labor Induction Phase 4
Withdrawn NCT00802646 - The Effects of Combined Spinal Epidurals on Fever During Labor of First-Time Mothers N/A
Completed NCT03903172 - Post-partum Non-pharmacologic Pain Management N/A
Recruiting NCT04955847 - Efficacy and Safety of Oral Misoprostol 25 μg vs. Vaginal Dinoprostone in Induction of Labor at Term
Completed NCT02824679 - Effect of Intravenous Hyoscine Butylbromide Injection on First Stage Labour in Primigavidae Phase 4
Completed NCT03264599 - Measurement of the Fetal Occiput-spine Angle During the First Stage of Labor as Predictor of the Outcome of Labor N/A
Completed NCT04543487 - Therapeutic Touch on Labour Pain, Anxiety and Childbirth Attitude N/A
Recruiting NCT02024256 - Cold Magnesium Sulfate Solution for Perineal Swelling Following Vaginal Delivery N/A
Recruiting NCT06426329 - The Effect of Therapeutic Touch at Birth on Pain, Birth Duration, Traumatic Birth Perception and Anxiety N/A
Not yet recruiting NCT06044129 - A Novel Approach Integrating Magnetic Resonance Imaging (MRI) Data and Artificial Intelligence for Predicting the Success Rate of Vaginal Delivery in Pregnant Women