Clinical trials: Misoprostol
Incomplete Abortion
Treatment of Incomplete Abortion With 600 Mcg Oral Misoprostol Compared to Standard Surgical Treatment
This study aims to compare the efficacy, side effects profile and acceptability of a single dose of 600mcg misoprostol taken orally compared to standard surgical treatment as per local protocols for the treatment of incomplete…
- Trial name
- NCT00674232
- Testing
- 600 mcg misoprostol, Surgical treatment
- Where
- 3 sites in Ecuador, Venezuela
- Volunteers
- 311 people, healthy volunteers welcome
- Sponsor
- Gynuity Health Projects
ıntrapartum Haemorrhage, Postpartum Haemorrhage
The Effect of Rectal and Sublingual Misoprostol Administration in Postpartum or Intrapartum Haemorrhage at Elective Caesarean Delivery: a Randomized Controlled Trial
The investigators hypothesis in this study is that administration of rectal and sublingual misoprostol decreases intrapartum and postpartum haemorrhage.
- Trial name
- NCT01931410
- Testing
- Misoprostol
- Volunteers
- 618 people
- Sponsor
- Istanbul Bakirkoy Maternity and Children Diseases Hospital
Gastric Ulcer
Evaluating PN 400 (VIMOVO) in Reducing Gastric Ulcers in High Risk Subjects Compared to Arthrotec
This randomized, double-blind, parallel-group, controlled, multi-center clinical trial of 6 months duration is designed to assess the efficacy, tolerability and safety of PN400 versus diclofenac/misoprostol in subjects at high…
- Trial name
- NCT00594854
- Testing
- PN400 (VIMOVO), Diclofenac/Misoprostol
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- POZEN
Neonatal Respiratory Distress
Vaginal Misoprostol to Improve the Neonatal Respiratory Outcome
Project summary: Objective: To test the hypothesis that administration of vaginal Misoprostol before elective cesarean section will improve the neonatal respiratory outcomes in late preterm and early term neonates through…
- Trial name
- NCT03239327
- Testing
- Misoprostol
- Where
- Egypt
- Volunteers
- 292 people
- Sponsor
- Assiut University
Pregnancy, Premature Rupture of Membranes
Cervical Ripening in Premature Rupture of Membranes
Premature rupture of membranes (PROM) is diagnosed by demonstrating amniotic fluid in the vaginal canal before the onset of labor.
- Conditions
- Pregnancy, Premature Rupture of Membranes, Preterm Premature Rupture of Membranes, Unfavorable Cervix
- Trial name
- NCT02314728
- Testing
- Misoprostol, Oxytocin
- Where
- United States
- Volunteers
- 230 people, healthy volunteers welcome
- Sponsor
- Montefiore Medical Center
Cesarean Section
Misoprostol Versus Active Management of Labour in CS
Several treatment strategies are emplemented to prevent post delivery hemorage and decreasing maternal morbidity and mortality .
- Trial name
- NCT03390010
- Testing
- Misoprostol + syntocinon and using extra uterotonic drugs when needed ; methergine, Syntocinon and using extra uterotonic drugs when needed ; methergine carboprost
- Where
- Egypt
- Volunteers
- 300 people, healthy volunteers welcome
- Sponsor
- Aljazeera Hospital
Postpartum Haemorrhage
Treatment of Postpartum Haemorrhage (PPH) Using Misoprostol in Home Births
A double-blind individual randomized controlled study of misoprostol vs. placebo for treatment in homebirths in the Chitral district, in the Khyber Pakhtunkhwa province in Pakistan.
- Trial name
- NCT01485562
- Testing
- Misoprostol
- Where
- Pakistan
- Volunteers
- 84 people, healthy volunteers welcome
- Sponsor
- Gynuity Health Projects
Incomplete Abortion
Misoprostol Treatment of Incomplete Abortion by Midwives and Physicians in Uganda
Uganda is one of the countries with highest fertility rate in the world, 6.7 children per women. It is estimated that 56 percent of all pregnancies are unintended and the contraceptive prevalence rate in Uganda is 23 percent.
- Trial name
- NCT01743508
- Testing
- Misoprostol treatment by midwife
- Where
- Uganda
- Volunteers
- 731 people
- Sponsor
- Karolinska Institutet
Labour Induction
The Misoprostol Vaginal Insert for Labour Induction
Objective: To compare the efficacy and safety of the misoprostol vaginal insert (MVI) for labour induction using standard (MVI-24) and adjusted (MVI-10) criteria. Design: Non-interventional observational case control study.
- Trial name
- NCT03016208
- Testing
- Misoprostol vaginal insert
- Volunteers
- 138 people
- Sponsor
- Asklepios Kliniken Hamburg GmbH
Pregnancy Related
Labor Induction With Double Balloon Device, Oral Misoprostol and Concomitant Use of Both
The aim of this study is to compare the rate of cesarean delivery between 3 methods of labor induction: double balloon device, oral misoprostol and combination of the two.
- Trial name
- IDOM (NCT03866772)
- Testing
- Misoprostol Oral Tablet, double balloon device for cervical ripening
- Where
- Israel
- Volunteers
- 250 people, healthy volunteers welcome
- Sponsor
- Bnai Zion Medical Center
Postpartum Hemorrhage
Comparison Between Preoperative Vaginal and Postoperative Sublingual Misoprostol for Prevention of Postpartum Hemorrhage During Cesarean Section
Cesarean section (CS) is one of the most frequently performed operative interventions worldwide [1]. Cesarean section rates increase each year throughout the world.
- Trial name
- NCT06765473
- Testing
- Misoprostol
- Volunteers
- 400 people
- Sponsor
- Assiut University
IUD Insertion Complication
Role of Vaginal Misoprostol Prior to IUCD Insertion in Women Who Delivered Only by Elective Caesarean Section.
Role of vaginal misoprostol prior to IUCD insertion in women who delivered only by elective caesarean section.
- Trial name
- NCT03939663
- Testing
- misoprostol
- Where
- Egypt
- Volunteers
- 210 people, healthy volunteers welcome
- Sponsor
- Ain Shams University
Hysteroscopy, Cervical Ripening
Significance of Misoprostol-induced Cervical Ripening Prior to Hysteroscopy
The goal of this prospective study is to evaluate the efficacy and safety of misoprostol for cervical ripening prior to hysteroscopy
- Trial name
- NCT06726278
- Testing
- Misoprostol 400mcg Tab
- Where
- Pakistan
- Volunteers
- 539 people
- Sponsor
- Hayat Abad Medical Complex, Peshawar
Intrauterine Fetal Demise
Misoprostol for Treatment of Fetal Death at 14-28 Weeks of Pregnancy
The purpose of the proposed study is to test - in a randomized, blinded trial - two different doses of the prostaglandin E1 analogue misoprostol administered buccally as a treatment for fetal death at 14 - 28 weeks, inclusive, of…
- Trial name
- NCT00671060
- Testing
- Misoprostol
- Where
- 5 sites in United States, Vietnam
- Volunteers
- 153 people
- Sponsor
- Gynuity Health Projects
Induction of Labor
Buccal Versus Vaginal Misoprostol In Combination With Foley Bulb
Combined misoprostol and Foley bulb catheter has been shown to be an effective induction method. However, optimal route of administration for misoprostol has not been established.
- Trial name
- BEGIN (NCT03976037)
- Testing
- Misoprostol
- Where
- United States
- Volunteers
- 216 people, healthy volunteers welcome
- Sponsor
- Christiana Care Health Services
Abortion, Induced
Cervical Preparation Before Dilation and Evacuation
The purpose of this research study is to compare three different ways of opening a woman's cervix before her second-trimester surgical abortion.
- Trial name
- NCT01751087
- Testing
- Mifepristone, misoprostol, Osmotic dilators
- Where
- 7 sites in United States
- Volunteers
- 300 people, healthy volunteers welcome
- Sponsor
- Planned Parenthood League of Massachusetts
Induction of Labor
Sublingual Versus Vaginal Misoprostol for Labor Induction at Term
Misoprostol (Cytotec®) is a synthetic prostaglandin E1 analog that has been marketed in the United States since 1988 as a gastric cytoprotective agent.
- Trial name
- NCT00140114
- Testing
- Misoprostol (Cytotec®)
- Where
- Lebanon
- Volunteers
- 170 people, healthy volunteers welcome
- Sponsor
- American University of Beirut Medical Center
Termed Pregnancy With Indications for Labor Induction.
Oral Versus Vaginal Misoprostol for Induction of Labor
The purpose of this study is to compare the efficacy between a single dose of oral misoprostol 100 microgram and vaginal misoprostol 50 microgram for induction of labor.
- Trial name
- NCT00148473
- Testing
- Misoprostol
- Where
- Thailand
- Volunteers
- 180 people, healthy volunteers welcome
- Sponsor
- Bangkok Metropolitan Administration Medical College and Vajira Hospital
Miscarriage
Management of Women With an Incomplete Miscarriage
Miscarriage is defined as the spontaneous loss of a pregnancy before 24 weeks' gestation, that is, before the fetal viability. The clinical signs of miscarriage are usually vaginal bleeding associated abdominal pain and cramping…
- Trial name
- NCT03148561
- Testing
- Misoprostol
- Where
- Egypt
- Volunteers
- 84 people
- Sponsor
- Assiut University
Abortifacient Agents, Nonsteroidal, Abortion, Incomplete
Misoprostol for Non-Viable Pregnancies
The purpose of this study is to examine the effectiveness of Misoprostol (Cytotec; GD Searle and Co., Chicago, IL) for the management of non-viable first trimester pregnancies.
- Conditions
- Abortifacient Agents, Nonsteroidal, Abortion, Incomplete, Misoprostol, Pregnancy
- Trial name
- NCT00426491
- Testing
- Misoprostol
- Where
- United States
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Madigan Army Medical Center