propranolol has been researched along with Dystocia in 3 studies
Propranolol: A widely used non-cardioselective beta-adrenergic antagonist. Propranolol has been used for MYOCARDIAL INFARCTION; ARRHYTHMIA; ANGINA PECTORIS; HYPERTENSION; HYPERTHYROIDISM; MIGRAINE; PHEOCHROMOCYTOMA; and ANXIETY but adverse effects instigate replacement by newer drugs.
propranolol : A propanolamine that is propan-2-ol substituted by a propan-2-ylamino group at position 1 and a naphthalen-1-yloxy group at position 3.
Dystocia: Slow or difficult OBSTETRIC LABOR or CHILDBIRTH.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (33.33) | 18.7374 |
1990's | 2 (66.67) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
UszyĆski, M | 1 |
Dulski, W | 1 |
Sanchez-Ramos, L | 1 |
Quillen, MJ | 1 |
Kaunitz, AM | 1 |
Adamsons, K | 1 |
de la Vega, A | 1 |
Santiago, P | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Propranolol Versus Placebo for Induction of Labor in Nulliparous Patients: a Double-blind Randomized Controlled Trial[NCT03348683] | Phase 2 | 240 participants (Actual) | Interventional | 2017-12-11 | Completed | ||
Propranolol for Prolonged Labor: A Randomized Controlled Trial (PRO-Labor Trial)[NCT04741698] | Phase 1 | 80 participants (Actual) | Interventional | 2021-07-27 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Time of latent labor defined as <6cm of cervical dilation. (NCT03348683)
Timeframe: average of 24 hours
Intervention | hours (Mean) |
---|---|
Propranolol | 11.0 |
Placebo | 11.2 |
Count of fetus with fetal bradycardia (<110bpm for >10 minutes within 30 minutes of study drug administration) (NCT03348683)
Timeframe: 30 minutes from drug administration
Intervention | Participants (Count of Participants) |
---|---|
Propranolol | 1 |
Placebo | 0 |
Count of fetus with fetal heart rate decelerations within 30 minutes of study drug administration (NCT03348683)
Timeframe: 30 minutes from drug administration
Intervention | Participants (Count of Participants) |
---|---|
Propranolol | 15 |
Placebo | 13 |
"Neonatal outcome - Number of neonates with hypoglycemia (blood glucose <50).~This population includes only the neonates who had heelsticks to check their blood glucose, which is not a universal practice and was not required by the protocol or IRB. The neonates included were those who met the nursery's risk-based protocol to check blood glucose after birth (ex: infants of diabetic mothers, fetal growth restriction, macrosomia, or symptoms suggestive of hypoglycemia)" (NCT03348683)
Timeframe: Day 1
Intervention | Participants (Count of Participants) |
---|---|
Propranolol | 11 |
Placebo | 8 |
"Composite neonatal outcome score was for any of the following morbidity: Neonatal Intensive Care Unit (NICU) admission, respiratory support (CPAP, nasal cannula, intubation), culture proven sepsis, radiographically proven intracranial hemorrhage, necrotizing enterocolitis, hypoglycemia (for those infants who had sugar checked), and neonatal death.~The composite score was computed as a score of 1 for any indication of neonatal morbidity - neonates who experienced at least one morbidity and the components are given equal weights. Patients who had no evidence of the predefined neonatal morbidities are subsequently given a score of 0. The minimum is 0 and maximum is 1." (NCT03348683)
Timeframe: Day 1
Intervention | Participants (Count of Participants) |
---|---|
Propranolol | 21 |
Placebo | 28 |
"Composite maternal morbidity score consists of a count of postpartum hemorrhage, transfusion, hysterectomy, placental abruption, chorioamnionitis, shoulder dystocia, episiotomy, higher order laceration, and ICU admission.~The composite score was computed as a score of 1 for any indication of maternal morbidity, that is the participant experienced at least one maternal morbidity, and the components are given equal weights. Participants who had no evidence of the predefined maternal morbidities are subsequently given a score of 0. The minimum is 0 and maximum is 1." (NCT03348683)
Timeframe: average of 24 hours
Intervention | Participants (Count of Participants) |
---|---|
Propranolol | 35 |
Placebo | 49 |
Greater than 500cc of blood expelled during a vaginal delivery or greater than 1000cc of blood expelled during a cesarean section (NCT03348683)
Timeframe: 30 minutes from drug administration
Intervention | Participants (Count of Participants) |
---|---|
Propranolol | 15 |
Placebo | 26 |
The time of induction (based on time of foley balloon placement for cervical ripening or misoprostol administration) to the time of delivery of the infant. (NCT03348683)
Timeframe: average of 24 hours
Intervention | hours (Mean) |
---|---|
Propranolol | 13.8 |
Placebo | 14.3 |
Number of various mode of delivery - count of Vaginal delivery, vacuum assisted vaginal delivery, forceps assisted vaginal delivery, cesarean section (NCT03348683)
Timeframe: average of 24 hours
Intervention | Participants (Count of Participants) | |||
---|---|---|---|---|
Spontaneous vaginal delivery | Vacuum assisted vaginal delivery | Forceps assisted vaginal delivery | Cesarean section | |
Placebo | 61 | 10 | 8 | 40 |
Propranolol | 64 | 3 | 8 | 46 |
2 trials available for propranolol and Dystocia
Article | Year |
---|---|
Randomized trial of oxytocin alone and with propranolol in the management of dysfunctional labor.
Topics: Adrenergic beta-Antagonists; Adult; Cesarean Section; Delivery, Obstetric; Double-Blind Method; Drug | 1996 |
Randomized trial of oxytocin alone and with propranolol in the management of dysfunctional labor.
Topics: Adrenergic beta-Antagonists; Adult; Cesarean Section; Delivery, Obstetric; Double-Blind Method; Drug | 1996 |
Randomized trial of oxytocin alone and with propranolol in the management of dysfunctional labor.
Topics: Adrenergic beta-Antagonists; Adult; Cesarean Section; Delivery, Obstetric; Double-Blind Method; Drug | 1996 |
Randomized trial of oxytocin alone and with propranolol in the management of dysfunctional labor.
Topics: Adrenergic beta-Antagonists; Adult; Cesarean Section; Delivery, Obstetric; Double-Blind Method; Drug | 1996 |
Reduction in the cesarean section rate in nulliparous patients after administration of intravenous propranolol.
Topics: Adrenergic beta-Antagonists; Adult; Apgar Score; Cesarean Section; Data Interpretation, Statistical; | 1999 |
1 other study available for propranolol and Dystocia
Article | Year |
---|---|
[Diagnosis and treatment of constriction ring dystocia].
Topics: Adult; Constriction, Pathologic; Dystocia; Female; Humans; Oxytocin; Pregnancy; Propranolol; Uterine | 1980 |