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Abortion, Induced clinical trials

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NCT ID: NCT04290832 Terminated - Abortion, Induced Clinical Trials

Developing and Testing Interventions to Address Conscientious Objection to Abortion Care in Mexico and South Africa

Start date: February 13, 2020
Phase: N/A
Study type: Interventional

The primary purpose of this research is to develop strategies and interventions to mitigate the impact of conscientious objection on women's access to safe abortion care in Mexico and South Africa using a user-centered design approach and test the feasibility and effectiveness of these interventions.

NCT ID: NCT03080493 Completed - Pain Clinical Trials

Gabapentin for Pain Control After Osmotic Dilator Insertion and Prior to D&E Procedure: a Randomized Controlled Trial

Start date: March 20, 2017
Phase: Phase 4
Study type: Interventional

Women having abortion procedures between 15 weeks 0 days and 23 weeks 6 days gestational age on the day of their procedure commonly have dilators placed in their cervix overnight before the abortion procedure. The dilators are put in during a pelvic exam in the clinic and after women go home they expand slowly overnight to open the cervix before the abortion procedure the next day. This can be a painful experience and health care providers often give women different kinds of pain medicine to help them. The investigators are interested in whether a medicine called gabapentin, which is a non-narcotic medicine, could help. Gabapentin is approved by the U.S. Food and Drug Administration (FDA) for prevention of seizures and for treating nerve pain and doctors are also using it to decrease pain for people having surgical procedures. The main goals of our study are to learn about: 1. Women's pain experience with dilators in their cervix overnight before the abortion procedure 2. How well gabapentin works to decrease women's pain while they have the dilators in their cervix Women who enroll in the study will get a dose of either gabapentin or placebo (a pill with no medicine in it) before their dilators are placed in the clinic. The medication they get (gabapentin or placebo) will be chosen by chance, like flipping a coin. Neither the women in the study nor the doctors giving them the medication will know which medication they receive so the investigators can learn about their pain without being influenced by knowing which medication they take. Doctors will be able to find out which medication women got if there is an emergency or if it changes their medical care. The investigators will communicate with women in real time overnight by text messaging to see how much pain they are having in the moment and how much pain medicine they are taking. The investigators hypothesize that women who receive gabapentin will have a smaller increase in their pain with the dilators than women who receive placebo (a pill with no medicine in it). The investigators' findings will help doctors understand women's pain experience with dilators better and possibly provide a new way of treating pain with gabapentin.

NCT ID: NCT02485444 Recruiting - Abortion, Induced Clinical Trials

Oxytocin Infusion vs. Spontaneous Follow-up for Third-stage of Labor After Second-trimester Abortion

Start date: June 2015
Phase: Phase 4
Study type: Interventional

This study compares oxytocin infusion to spontaneous follow-up for third-stage of labor at induced mid-trimester abortions. Patients will be randomized to oxytocin infusion or observation with no pharmacologic intervention. Primary outcome of the study is complete abortion rate within two hours of fetal delivery.

NCT ID: NCT02480543 Recruiting - Abortion, Induced Clinical Trials

Different Routes of Misoprostol Prior to First Trimester Surgical Abortion

Start date: July 2015
Phase: Phase 4
Study type: Interventional

A randomized clinical trial to assess the effectiveness of same-day cervical preparation with oral, buccal or vaginal Misoprostol, given 2-4 hours prior first trimester curettage.

NCT ID: NCT02318212 Completed - Abortion, Induced Clinical Trials

Dilapan-S / Dilasoft E-Registry in Induced Abortion

Start date: March 2015
Phase: N/A
Study type: Observational

International Observational E-Registry on the use of osmotic dilators DILAPAN-S® / DILASOFT® for cervical priming prior to induced abortion.

NCT ID: NCT02279914 Completed - Abortion, Induced Clinical Trials

Misoprostol Dose and Timing Before Surgical Abortion at 13 to 16 Weeks' Gestation: a Randomized Trial

Start date: November 2014
Phase: N/A
Study type: Interventional

This study is a blinded randomized trial to compare two different doses and intervals of buccal misoprostol for cervical preparation before surgical abortion at 13 to 16 weeks' gestation: 400 mcg administered 3 hours before D&E (dilation and extraction), and 600 mcg administered 1.5 hours before D&E. Primary objective: To compare operative times after two different doses and intervals of misoprostol using a non-inferiority design. Secondary objectives: To compare the doses and intervals of misoprostol for differences in: (1) initial cervical dilation; (2) need for mechanical dilation and ease of dilation if required; (3) ability to complete the abortion procedure without further cervical preparation; (4) complications; (5) provider variables including ease of procedure and satisfaction with cervical preparation; (6) patient variables including pre-operative side effects, post-operative pain, and acceptability

NCT ID: NCT02277249 Completed - Abortion, Induced Clinical Trials

Transvaginal Versus Transabdominal Digoxin Prior to Second-trimester Abortion

Start date: October 2012
Phase: N/A
Study type: Interventional

Current practice for the provision of late second trimester abortion (dilation and evacuation, or D&E) often involves the administration of digoxin into the fetal compartment to induce fetal demise prior to the procedure. Digoxin may be administered transabdominally or transvaginally into the fetal compartment. Both modes of administration have been shown in prospective studies to be highly effective and safe. Both modes of administration are considered standard of care. This pilot study will directly compare transabdominal and transvaginal digoxin with respect to patient preference (i.e, patient pain score describing discomfort with injection).

NCT ID: NCT02048098 Completed - Abortion, Induced Clinical Trials

Misoprostol for Second Trimester Termination of Pregnancy

Start date: January 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the efficacy of 400 µg vaginal misoprostol per 3 hours to 400 µg buccal misoprostol per 3 hours in second trimester termination of viable pregnancy

NCT ID: NCT01751087 Completed - Abortion, Induced Clinical Trials

Cervical Preparation Before Dilation and Evacuation

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

The purpose of this research study is to compare three different ways of opening a woman's cervix before her second-trimester surgical abortion. - Osmotic dilators: small rods that, when inserted into the cervix, gently expand to open the cervix - Osmotic dilators plus mifepristone, a medicine that is swallowed - Osmotic dilators plus misoprostol, a medicine that is placed between the cheek and gum Hypotheses: - adding buccal misoprostol 3 hours preoperatively will significantly improve dilation compared to laminaria alone, making procedures faster, easier and safer. - adding oral mifepristone at the time of laminaria placement will confer a similar benefit. - the efficacy of adjunctive misoprostol and mifepristone will be influenced by gestational age, with women later in gestation having increased efficacy from these agents. - significantly more patients who receive adjunctive misoprostol or mifepristone will have adequate initial dilation, fewer will require manual dilation or additional cervical preparation and there will be fewer complications in these arms, although complication rates will be low and we will only be able to detect relatively large differences. - patients will prefer to have the procedure done as quickly as possible with as little discomfort as possible, that cervical ripening with adjunctive misoprostol will be associated with more cramping than osmotic dilators alone and that mifepristone will be well tolerated and may not cause more cramping or other side effects than osmotic dilators alone.

NCT ID: NCT01615731 Completed - Abortion, Induced Clinical Trials

Value of Mifepristone in Cervical Preparation Prior to Dilation and Evacuation 19-24 Weeks

Start date: May 2012
Phase: N/A
Study type: Interventional

A common practice for preparation for surgical abortion after 19 weeks gestation is the placement of multiple sets of osmostic dilators 1-2 days prior to the procedure. The investigators aim to study the addition of mifepristone as an adjunct to cervical dilation prior to abortion between 19-24 weeks gestation, and its potential to minimize the number of painful procedures and time in clinic (or away from work/home) that multiple sets of dilators can require. The investigators hypothesize that one set of dilators with mifepristone will result in similar procedure times and decreased "total" time as two sets of dilators.