Clinical trials

6

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Once-Daily vs Twice-Daily Insulin Glargine in Pregestational Diabetes Management

The purpose of this study is to determine if taking insulin glargine twice a day instead of once a day will better manage pregestational diabetes in pregnant patients. Participants in this study will be randomly assigned to one of two groups: a group that takes insulin glargine once a day, and a group that takes it twice. Continuous glucose monitoring will be used to track blood sugar levels. The main question the study aims to answer is: Will using insulin glargine twice a day instead of once lead to a better glucose time in range?

Participants needed: 200
Trial details
Phase: Phase 4Age: 18+Biological sex: FemaleType: InterventionalSponsor: Eastern Virginia Medical SchoolUpdated: May 15, 2026Locations: 1
Eligibility criteria

Patients older than 18 years of age; [+4]

Known allergy or reaction to insulin glargine, or concurrent medical condition w... [+4]

Status: Not yet recruiting

Glucose Control in Type 2 Diabetes in Pregnancy

The goal of this clinical trial is to evaluate the effect of physical activity on glucose control in pregnant patients with pregestational Type 2 diabetes. The main question it seeks to answer is "will physical activity following a meal improve blood sugar control in pregnant women with Type 2 diabetes?" Researchers will compare the glucose control of two groups: one that walks for 20 minutes after each meal, and one that does not.

Participants needed: 40
Trial details
Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Eastern Virginia Medical SchoolUpdated: Nov 26, 2025Locations: 1
Eligibility criteria

Singleton gestation [+3]

Non-English as the primary language [+4]

Status: Recruiting

Lactated Ringer's and Dextrose 5% vs Only Lactated Ringer's in Labor

The goal of this clinical trial is to determine which of two types of standard intravenous (IV) fluids (a combination of 5% dextrose and Lactated Ringers solution and Lactated Ringers solution alone) has a better influence on labor when inducing labor in pregnant women. The main questions it aims to answer are: 1. Does the use of 5% dextrose and Lactated Ringers lead to a shorter labor than the use of just Lactated Ringers? 2. Does the use of 5% dextrose and Lactated Ringers increase the risk of neonatal hypoglycemia when compared to Lactated Ringers? Participants in this trial will be randomly assigned to one of two groups: a group that receives a solution of 5% dextrose and Lactated Ringers, and a group that receives Lactated Ringers alone. Researchers will compare the outcomes of the two groups to see which IV fluid is more effective.

Participants needed: 158
Trial details
Phase: Phase 4Age: 18+Biological sex: FemaleType: InterventionalSponsor: Eastern Virginia Medical SchoolUpdated: Aug 22, 2025Locations: 2
Eligibility criteria

Nulliparous women [+5]

Age under 18 years [+12]

Status: Recruiting

Oxytocin/Foley vs. Oxytocin for Induction in Patients With PPROM

Data on the optimal mode of labor induction after preterm prelabor rupture of membranes (PPROM) is lacking. Studies have shown no difference between oxytocin and misoprostol use for labor induction in this cohort (1). The preponderance of evidence from term pregnancies suggests that Foley catheter coupled with oxytocin is better than oxytocin alone, with a higher rate of delivery within 24 hours when a Foley catheter followed by oxytocin is compared to oxytocin alone. However, the use of a Foley catheter has not been evaluated in prospective studies on patients with PPROM.

Participants needed: 80
Trial details
Phase: Phase 4Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Eastern Virginia Medical SchoolUpdated: Aug 13, 2025Locations: 1
Eligibility criteria

Patients 18-50 years of age; [+5]

Spontaneous labor [+7]

Status: Recruiting

Effect of Fiber Supplementation on the Need for Medication With Gestational Diabetes

The hypotheses to be tested are 1) Fiber supplementation will decrease the need for medication in patients with gestational diabetes, and 2) Fiber supplementation will decrease adverse maternal and neonatal outcomes in these patients. In this study, the investigators will conduct a randomized controlled trial to limit bias in evaluating these hypotheses.

Participants needed: 110
Trial details
Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Eastern Virginia Medical SchoolUpdated: Mar 10, 2025Locations: 1
Eligibility criteria

Singleton gestation [+2]

- Non-English as primary language. [+5]

Status: Recruiting

Effects of THC-Free CBD Oil on Agitation in Patients With Alzheimer's Disease

This is a randomized, double-blinded, placebo-controlled, crossover trial that aims to 1) determine the efficacy of THC-free cannabidiol (CBD oil) in reducing the severity of agitation among participants and 2) determine whether THC-free CBD oil can reduce the burden on caregivers and increase the participants' quality of life.

Participants needed: 40
Trial details
Phase: Phase 2Age: 50-90Biological sex: AllType: InterventionalSponsor: Eastern Virginia Medical SchoolUpdated: Feb 16, 2023Locations: 1
Eligibility criteria

Males/females over 50 years old. [+6]

Diagnosis of non-AD or non-mixed dementias. [+15]