Baltimore, MDNCT06199154Now EnrollingIRB Ready

Morbid Obesity Clinical Trial in Baltimore, MD

Access cutting-edge morbid obesity treatment through this clinical trial at a research site in Baltimore. Study-provided care at no cost to qualified participants.

Sponsored by University of Maryland, Baltimore

Quick Self-Assessment

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Expert Care in Baltimore

Access morbid obesity specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related morbid obesity treatment provided free

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Check if you qualify for this morbid obesity clinical trial in Baltimore, MD

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Baltimore

    Convenient for MD residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Baltimore site if eligible
  4. 4Begin participation

About This Morbid Obesity Study in Baltimore

The goal of this randomized control trial is to compare different doses of Misoprostol (25 mcg vs 50 mcg) in induction of labor (IOL) in morbidly obese patients with BMI \>40. It is known that morbid obesity is a risk factor for failed IOL and ultimately cesarean delivery (CD.) If the rates of vaginal delivery in this population can improve, then surgical morbidity can be reduced in these patients.

Sponsor: University of Maryland, Baltimore

Who Can Participate

Inclusion Criteria

Morbidly obese (BMI ≥ 40 kg/m2) at admission for induction of labor
Speaks English or Spanish
Gestational age between 34 weeks and 0 days and 42 weeks and 6 days
Age 18 years old or older
Viable, single, cephalic fetus
Intent to proceed with cervical ripening - cervical exam: dilation \< 5 cm
Contractions \< 5 per 10 minutes

Exclusion Criteria

History of cesarean delivery
Contraindication to prostaglandin administration (significant myomectomy, prior cesarean delivery)
Contraindication to vaginal delivery (placenta previa, vasa previa, HIV with high viral load)
Contraindications to labor (cardiac, neurosurgical, need for cesarean)
Age \< 18yo
Fetal growth restriction with abnormal umbilical artery Doppler indices
Cervical dilation \>5 cm
Contractions \>5 per 10 minutes
Significant vaginal bleeding with concern for placental abruption
Non-reassuring fetal status or fetal heart rate decelerations
Fetal demise or major fetal anomaly
Inability to give consent

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Baltimore?

Yes, this clinical trial (NCT06199154) has an active research site in Baltimore, MD that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Morbid Obesity Treatment Options in Baltimore, MD

If you're searching for morbid obesity treatment options in Baltimore, MD, this clinical trial (NCT06199154) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Baltimore research site is actively enrolling participants for this clinical trial. You'll receive care from experienced morbid obesity specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all morbid obesity clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Baltimore, MD