Abortion. Spontaneous abortion Incomplete, without complication
Conditions
Interventions
Intervention 1: Intervention group: The study group consists of 46 individuals, with 23 undergoing their first cesarean section and 23 undergoing their second or more cesarean section, all of whom wil
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Pregnant women who, for any reason, are unable to continue their pregnancy and require an abortion. Being in the first or second trimester of pregnancy. Mothers with a history of one or two previous cesarean sections.
Exclusion criteria
Exclusion criteria: Unwillingness to cooperate and participate in the study Any cervical lesion that could affect the results (e.g., fibroid, cervical insufficiency, etc.). Cardiovascular patients using nitrate medications and/or with respiratory complications. Hemorrhagic disorders. Patients who are taking aspirin and/or heparin. Having an autoimmune disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of the abortion procedure. Timepoint: Every three hours. Method of measurement: Clinical examination. | — |
Secondary
| Measure | Time frame |
|---|---|
| Complications after abortion, including rupture uterus and severe bleeding. Timepoint: After abortion. Method of measurement: clinical examination. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNasim Solemani
Shiraz University of Medical Sciences
Outcome results
None listed