Guanfacine and Cromolyn Sodium for POTS: The DBPOTS Trial

Trial statusNot yet recruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18-100
SponsorJohns Hopkins University

About this trial

The goal of this clinical trial is to learn whether guanfacine or cromolyn sodium can improve symptoms and physical functioning in adults with Postural Orthostatic Tachycardia Syndrome (POTS). Both medications are FDA-approved for other conditions but are investigational for the treatment of POTS.

The main questions this study aims to answer are:

Does treatment with guanfacine or cromolyn sodium improve physical functioning in adults with POTS compared with placebo? Does treatment with guanfacine or cromolyn sodium improve fatigue, cognitive function ("brain fog"), gastrointestinal symptoms, and overall symptom burden in adults with POTS?

Researchers will compare guanfacine, cromolyn sodium, and placebo to determine whether either active treatment provides greater improvement in symptoms and physical functioning than placebo.

Participants will:

Be randomly assigned to receive guanfacine, cromolyn sodium, and placebo during separate 4-week treatment periods in a randomized, double-blind crossover study.

Continue standard non-drug POTS management, including recommendations for fluid and salt intake, exercise, compression garments, and other lifestyle measures.

Complete questionnaires that measure physical function, fatigue, cognitive symptoms, gastrointestinal symptoms, and overall health throughout the study.

Attend scheduled study visits for safety monitoring and assessment of study outcomes.

Provide blood, urine, and sputum samples so researchers can evaluate biomarkers related to POTS and better understand how these treatments may work.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

a heart rate increase of ≥30 bpm within the first 10 minutes of standing or tilt-table testing, without orthostatic hypotension (systolic BP drop ≥20 mmHg)

Frequent symptoms of orthostatic intolerance (e.g., dizziness, palpitations, GI complaints) persisting ≥3 months

Symptom onset within 3 months of a recognized POTS trigger (e.g., infection, vaccination, injury, surgery, pregnancy, or puberty)

Symptomatic response to mediator-targeting medications (e.g., antihistamines, mast cell stabilizers) - also eligible

Disqualifiers

Anemia,

Active infection,

Dehydration,

Hyperthyroidism,

Trial design

Design model

Crossover

Treatments tested in this trial

  • Guanfacine (GFC)

    Drug

    Participants receive oral guanfacine for 4 weeks while continuing standardized non-pharmacologic management of POTS. Guanfacine is initiated at 1 mg once daily and may be increased to 2 mg once daily at Week 3 if adequate clinical improvement has not been achieved and the medication is well tolerated. Participants complete symptom assessments and safety evaluations throughout the treatment period.

  • Cromolyn Sodium

    Drug

    Participants receive oral cromolyn sodium for 4 weeks while continuing standardized non-pharmacologic management of POTS. Treatment begins at 200 mg twice daily (400 mg/day) and may be increased to 400 mg twice daily (800 mg/day). For participants who tolerate treatment but have an inadequate response, the dose may be further increased to 1,600 mg/day according to the protocol. Symptom assessments and safety evaluations are performed throughout the treatment period.

  • Placebo

    Drug

    Participants receive matched placebo for 4 weeks while continuing standardized non-pharmacologic management of POTS. Placebo products are matched to the active study medications, including identical dose-escalation procedures, to maintain blinding. Participants complete the same symptom assessments and safety evaluations as during the active treatment periods.

Treatment groups

25 Participants
are divided into 3 treatment groups
Group A: GuanfacineExperimental treatment 3 interventions
Group B: Cromolyn SodiumExperimental treatment 3 interventions
Group C: PlaceboPlacebo comparator 3 interventions

Trial outcomes

Primary outcomes

1

Change in Physical Function as Measured by the PROMIS® Physical Function Scale

Scores are reported as T-scores based on a U.S. population average of 50, with a standard deviation of 10. Higher scores indicate better physical function.

Time frame
Week 0 (baseline), Week 4 (end of treatment), week 10 (end of treatment), week 16 (end of treatment)

Secondary outcomes

1

Patient-Reported Outcomes Measurement Information System (PROMIS®) Fatigue

T-score (mean = 50, SD = 10). Higher T-scores indicate greater fatigue (worse outcome).

Time frame
Week 0 (baseline), Week 4 (end of treatment), week 10 (end of treatment), week 16 (end of treatment)
2

Patient-Reported Outcomes Measurement Information System (PROMIS®) Cognitive Function

T-score (mean = 50, SD = 10). Higher T-scores indicate better cognitive function (better outcome).

Time frame
Week 0 (baseline), Week 4 (end of treatment), Week 10 (end of treatment), Week 16 (end of treatment)
3

Clinical Global Impressions (CGI)

Score ranges from 1 to 7. Higher scores indicate greater illness severity or worsening (worse outcome).

Time frame
Week 0 (baseline), Week 4 (end of treatment), Week 10 (end of treatment), Week 16 (end of treatment)
4

Malmö Postural Orthostatic Tachycardia Syndrome Symptom Score

Total score ranges from 0 to 120. Higher scores indicate greater POTS symptom burden (worse outcome).

Time frame
Week 0 (baseline), Week 4 (end of treatment), Week 10 (end of treatment), and Week 16 (end of treatment)

Other outcomes

Sponsors and contacts

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Johns Hopkins University

Lead sponsor

Dysautonomia International

Collaborator

This trial is not recruiting at the moment. You can still explore other options: