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Endometritis clinical trials

View clinical trials related to Endometritis.

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NCT ID: NCT04432467 Completed - Clinical trials for Chronic Endometritis

Fertility Restoration Using Autologous Mesenchymal Stem Cells

Start date: October 1, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

Treatment of the patients with scarring and adhesions in the uterus resulting from caesarean section or chronic inflammation in the mucosa of the uterus and fallopian tubes and preventing the occurrence of these effects in the future

NCT ID: NCT04385680 Completed - Wound Infection Clinical Trials

Chlorhexidine Vaginal Preparation for Reduction of Post-cesarean Endometritis and Sepsis

Start date: May 15, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

The study aims to assess the beneficial value of vaginal preparation with chlorhexidine gluconate 0.05% before cesarean delivery of cases in labor in reduction of postoperative endometritis, fever and wound complications compared to no preparation or using saline only.

NCT ID: NCT04307069 Recruiting - Clinical trials for Cesarean Section Complications

Management of Prelabor Rupture of the Membranes at Term

Start date: May 1, 2020
Phase: N/A
Study type: Interventional

Prolonged rupture of membranes has been associated with increased risk of chorioamnionitis and endometritis. In this study the investigators will investigate whether an early intervention to augment labor with oxytocin is superior to expected management for spontaneous delivery (up to 24 hours).

NCT ID: NCT04197167 Recruiting - IVF Clinical Trials

Mid-Infrared Spectroscopy as a Real Time Diagnostic Tool for Chronic Endometritis

Start date: December 12, 2019
Phase: N/A
Study type: Interventional

The Investigator propose to develop an in-vitro technique for the measurement and analysis of freshly excised biopsies during hysteroscopy procedure in patients with suspected Chronic Endometritis (CE) condition. Furthermore, the investigator propose to develop a discrimination model between the CE and inflammatory CE types using the measured spectroscopic data from freshly excised biopsies.

NCT ID: NCT04163679 Terminated - Infection Clinical Trials

Vaginal Preparation and Azithromycin to Reduce Post Cesarean Infections

Start date: September 18, 2019
Phase: N/A
Study type: Interventional

asdgf

NCT ID: NCT04103242 Not yet recruiting - Infertility, Female Clinical Trials

Abundance of Lactobacillus in Endometrium Affected by Chronic Endometritis

endoMB
Start date: July 1, 2020
Phase:
Study type: Observational

Infertile women undergoing hysteroscopy for diagnostic or therapeutic indication are asked to donate a sample of endometrium. Endometrial samples of study participants are examined for signs of chronic endometritis by immunohistochemical analysis. High-throughput sequencing of the microbial 16s ribosomal ribonucleic acid (rRNA) subunit is performed to identify and quantify the microbes present in the sample. Obstetric and reproductive outcome is recorded 12 months after hysteroscopy (telephone interview).

NCT ID: NCT03960970 Recruiting - Wound Infection Clinical Trials

Two-drug Antibiotic Prophylaxis in Scheduled Cesarean Deliveries

Start date: September 15, 2019
Phase: Phase 2
Study type: Interventional

Cesarean deliveries are the most common surgical procedure performed in the United States. A significant decrease in cesarean delivery associated maternal morbidity has been achieved with preoperative prophylactic single-dose cephalosporin, widely used before skin incision. Also, on laboring patients and/or with rupture of membranes, several studies suggest that adding azithromycin to standard cephalosporin prophylaxis is cost-effective and reduces overall rates of endometritis, wound infection, readmission, use of antibiotics and serious maternal events. Azithromycin has effective coverage against Ureaplasma, associated with increased rates of endometritis. Although two-drug regimen has been suggested for laboring and/or patients that undergo cesarean delivery, no studies have investigated the potential benefits of two-drug regimen in non-laboring patients.

NCT ID: NCT03840889 Not yet recruiting - Clinical trials for Postpartum Hemorrhage

Secondary Postpartum Hemorrhage

SPPH
Start date: March 1, 2019
Phase:
Study type: Observational

Postpartum hemorrhage (PPH) remains one of the leading causes of maternal mortality and morbidity worldwide, including in France, where it accounts for approximately 20% of maternal mortality. Although numerous studies have examined immediate PPH, very few have explored secondary (also called late) PPH. Moreover, there are no guidelines in France for the management of secondary PPH. Its frequency appears to vary from 0.2% to 3.0% of deliveries. It is, however, difficult to estimate because only severe secondary PPH will lead to hospitalization and the rare publications concern single-center studies. The cause of these secondary hemorrhages is often unknown, due to the lack of routine uterine aspiration. Nonetheless, this aspiration is not always medically justified. The principal objective of this study is thus to establish the incidence of severe late PPH in the general population.

NCT ID: NCT03478163 Terminated - Clinical trials for Postpartum Hemorrhage

Antibiotics During Intrauterine Balloon Tamponade Placement

Start date: March 8, 2018
Phase: Phase 4
Study type: Interventional

The goal of this study is to identify whether antibiotics given at the time of placement of an intrauterine balloon tamponade (IBT) will result in reduction of the risk of endometritis. The investigators hypothesize that antibiotics given at the time of intrauterine balloon tamponade will reduce the likelihood of postpartum endometritis.

NCT ID: NCT03459599 Completed - Endometritis Clinical Trials

Antibiotic Prophylaxis in Ragged Placental Membranes

Start date: October 1, 2016
Phase: N/A
Study type: Interventional

In some centres, women are routinely given a course of antibiotics postnatally if ragged placental membranes were present at delivery. The investigators examined the necessity such an intervention.