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Second Trimester Abortion clinical trials

View clinical trials related to Second Trimester Abortion.

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NCT ID: NCT06164067 Completed - Clinical trials for Second Trimester Abortion

The Role of Cervical Consistency Index and Uterocervical Angles in Medical Termination

Start date: February 15, 2022
Phase:
Study type: Observational [Patient Registry]

The main aim of the investigator study is the success of predictivity cervical consistency index (CCI), anterior uterocervical angle (aUCA) and posterior uterocervical angle (pUCA) in second trimester terminations.

NCT ID: NCT04181541 Completed - Medical Abortion Clinical Trials

Midlevel Versus Physician-provided Medical Abortion in the Second Trimester

Start date: February 17, 2020
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the safety and effectiveness of second trimester medical abortion when provided by nurse midwives compared with physicians. The study sample will be obtained from Michu Clinic, affiliated with St Paul's hospital, in Addis Ababa.

NCT ID: NCT03407521 Completed - Clinical trials for Second Trimester Abortion

Misoprosotol and Isosorbide Mononitrate for Induction of Second Trimester Abortion

Start date: April 12, 2017
Phase: Phase 4
Study type: Interventional

the investigators aimed to study the efficacy and safety of nitric oxide donors when combined with prostaglandins in induction of second trimester abortion expecting that both drugs when used together will be of greater efficiency and associated with less side effects. the study included 60 women with gestational age between 13weeks+0day and 26weeks+6days indicated for pregnancy termination due to maternal or fetal cause.

NCT ID: NCT03400358 Completed - Clinical trials for Medical; Abortion, Fetus

Uterocervical Angle in the Pregnancy Termination of Multiparous Women

Start date: October 1, 2017
Phase: N/A
Study type: Observational

To evaluate the uterocervical angle (UCA) in the prediction of second trimester termination success of multiparous women.

NCT ID: NCT02033083 Completed - Clinical trials for Second Trimester Abortion

Laminaria Compared to Dilapan-S for Cervical Preparation Before Dilation and Evacuation at 18-24 Weeks of Gestation

Start date: December 2013
Phase: N/A
Study type: Interventional

Primary objective: To study the difference in dilation and evacuation (D&E) procedure time following overnight cervical preparation with laminaria or Dilapan-S™. The investigators hypothesize procedure time will be less with Dilapan-S™. Secondary objectives: To compare the use of laminaria and Dilapan-S™ for differences in: (1) initial cervical dilation before D&E; (2) need for mechanical dilation to accomplish D&E and ease of dilation if required; (3) number of osmotic dilators placed; (4) ability to complete the D&E procedure without further cervical preparation; (5) complications; (6) pain and other side effects; (7) patient acceptability; and (8) provider acceptability.