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Vasopressin Analog

Desmopressin for Bedwetting

Phase 4
Waitlist Available
Led By Kerry Morrone, MD
Research Sponsored by Montefiore Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline and 4 weeks
Awards & highlights

Study Summary

This trial will see if desmopressin helps sickle cell patients stop nighttime bedwetting.

Eligible Conditions
  • Bedwetting
  • Sickle Cell Anemia

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline and 4 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline and 4 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in Bedwetting episodes
Secondary outcome measures
Change in Daytime Fatigue
Change in Nighttime awakenings
Impact of Bedwetting on day to day activities

Side effects data

From 2012 Phase 3 trial • 395 Patients • NCT01262456
5%
Headache
2%
Hyponatraemia
1%
Osteoarthritis
1%
Acute myocardial infarction
100%
80%
60%
40%
20%
0%
Study treatment Arm
Desmopressin 50 μg Double-Blind
Desmopressin 75 μg Double-Blind
Placebo Double-Blind
Desmopressin 50 μg Double-Blind / 100 μg Open-Label
Desmopressin 75 μg Double-Blind / 100 μg Open-Label
Placebo Double-Blind / Desmopressin 100 μg Open-Label

Trial Design

1Treatment groups
Experimental Treatment
Group I: Treatment GroupExperimental Treatment1 Intervention
Desmopressin 0.2mg tablets, dose titrated to effect
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Desmopressin
2010
Completed Phase 4
~3990

Find a Location

Who is running the clinical trial?

Montefiore Medical CenterLead Sponsor
441 Previous Clinical Trials
582,189 Total Patients Enrolled
Kerry Morrone, MDPrincipal Investigator - Montefiore Medical Center
Children's Hospital at Montefiore, The, Montefiore Medical Center, Montefiore Medical Center-North
1 Previous Clinical Trials
3 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are presently enrolling volunteers for the trial?

"Clinicaltrials.gov denotes that this study, initially posted on July 7th 2020, is presently recruiting patients. The trial has been edited as recently as May 25th 2022."

Answered by AI

Who is eligible to join this research project?

"In order to be eligible for this trial, one must suffer from nocturnal enuresis and should lie between 8-21 years of age. The study is currently accepting around 60 participants."

Answered by AI

Are there any documented precedents of research involving Desmopressin?

"Presently, there is one active clinical trial assessing the efficacy of Desmopressin. This medical investigation has yet to reach Phase 3 and is predominantly located in Bronx, New york with a single additional site."

Answered by AI

Is the age range for participants in this trial inclusive of individuals over 75 years old?

"According to the study parameters, individuals eligible for this trial must be between 8 and 21 years old. Meanwhile, there are 148 studies open for participants younger than 18 and 214 trials available for those over 65."

Answered by AI

What indications is Desmopressin typically used to treat?

"Desmopressin may prove beneficial in treating von willebrand disease, as well as haemorrhaging and polyuria."

Answered by AI

How many participants are currently enrolled in this scientific research?

"Affirmative. According to clinicaltrials.gov, this research study is actively enrolling members of the public after its original posting on July 7th 2020 and latest update on May 25th 2022. To complete their experiment, the team needs 60 participants from a single site."

Answered by AI

Is Desmopressin a viable option for medical treatment with minimal risk?

"The safety of Desmopressin has been positively established, hence it is assigned a rating of 3. This Phase 4 trial confirms that this medication has already been approved for use."

Answered by AI
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~1 spots leftby Apr 2025