Skip to content

Comparative study oneffect of Nitroglycerin and Misoprostol oncervical ripeningbefore curettage in women

The surveya comparative study on the effect of Nitroglycerin and Misoprostol oncervical ripening before first-trimester curettage in women (aclinical trial)

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210510051247N1
Enrollment
170
Registered
2021-05-16
Start date
2021-05-22
Completion date
Unknown
Last updated
2021-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy ,Medical abortion, Nitroglycerin ., Misoprostol ,cervical ripening. XV Pregnancy, childbirth and the puerperium ,Medical abortion

Interventions

Intervention 1: Intervention groups: Group A 85 people will receive 400 mg single dose of trinitroglycerin tablets of Dana Pharmaceutical Company vaginally. Intervention 2: Intervention group: Group B

Sponsors

Rasht University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: After obtaining full consent to participate in the study, pregnant women are candidates for curettage with a gestational age of less than 14 weeks who have a reason for termination of pregnancy (missed abortion, medical abortion) based on the case file documents And have normal vital signs including no fever( less than 38 ° C), normal heart rate between 70 and 100 and systolic blood pressure between 100 and 130. Also have a history of uterine scarring at most once, no drug abuse, no bleeding (based on initial examination )Lack of coagulation disorder or recent history of anticoagulants, no active liver disease, cardiovascular disease, uncontrolled seizures, history of glaucoma, adrenal insufficiency are the conditions for inclusion in the study.

Exclusion criteria

Exclusion criteria: Patients who wish to have a medical abortion and are not candidates for curettage surgery for any reason. Women who have more than one history of uterine scarring are not included in the study

Design outcomes

Primary

MeasureTime frame
Cervical ripening. Timepoint: Initial examination and 4 hours after receiving the drug. Method of measurement: Hegar Bogey No. 8 passes through the cervix.

Secondary

MeasureTime frame
Requires mechanical dilatation. Timepoint: During curettage. Method of measurement: HegarBogey No. 8 passes through the cervix.;Possible side effects (diarrhea, chills, abdominal pain, headache, hypotension and palpitations). Timepoint: Every 4 hours during hospitalization. Method of measurement: Questioning the patient, examination, control of vital signs.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGhazaleh Ghorbani

Rasht University of Medical Sciences

gh.ghorbani7012@gmail.com+98 13 3336 9224

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026