RecruitingPhase 2

Pyridostigmine for the Treatment of Constipation in Parkinson Disease

Who can join

As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.

Age
18 Years and older
Sex
All sexes
Healthy volunteers
Not accepted
Compensation
Not stated

Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.

What to expect

No one can promise a trial will help you personally — that is what the research is trying to find out.

What participation involves

Not stated in the study description — ask the study team about visits and procedures.

Compensation
Not stated
  • Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
  • Participants are monitored closely by the research team throughout the study.
  • Some participants may receive access to an investigational treatment, which is still being studied.
  • Your participation helps researchers learn whether this approach could help future patients.

About this study

In plain language

This study tests whether pyridostigmine is safe and helps treat long-term constipation in people with Parkinson disease. It is for adults who have Parkinson disease and have trouble passing stool.

Constipation is a common and debilitating non-motor symptom of Parkinson disease (PD) that often precedes the onset of classic motor symptoms by decades. There is no standardized algorithm for managing constipation in this patient population, nor are there dedicated treatments. Studies suggest that constipation can affect quality of life to a significant degree, in many cases just as much as motor symptoms. There is an unmet need for effective treatment options for constipation in this patient population. The goal of this study is to determine the efficacy and safety of pyridostigmine as a treatment for chronic constipation in patients with PD.

Compensation is read from the study's own description and may be missing — always confirm with the study team.

Eligibility

Who can join

  • Be at least 18 years old.
  • Be able to sign a form agreeing to join the study.
  • Be willing and able to follow all study steps and take medicine by mouth.
  • Have Parkinson disease that meets the study’s diagnosis rules, including slow movement and other required signs.
  • Have three or fewer bowel movements a week, plus another constipation symptom, such as hard stools, straining, feeling blocked, or needing help to pass stool.
  • Meet the study’s constipation rules for at least 3 months, with symptoms starting at least 6 months before diagnosis. Loose stools must be rare without laxatives, and symptoms must not meet the rules for irritable bowel syndrome.
  • Sexually active women who can become pregnant must use two approved birth control methods, or one approved method plus a partner’s condom, during the study and for 28 days after the last study drug dose.
  • Sexually active men who can father a child must use condoms during the study and for 28 days after the last study drug dose. Their partner must use approved birth control or have gone through menopause.

Who can't join

  • Have an unusual form of Parkinson-like illness, or one caused by medicines or blood vessel problems.
  • Have an allergy to pyridostigmine or any study drug ingredient, or have used pyridostigmine within 90 days before joining.
  • Have ever had bowel surgery or a blocked bowel or bladder.
  • Have severe asthma or chronic obstructive pulmonary disease (COPD), a long-term lung disease.
  • Have other findings that rule out Parkinson disease under the study’s diagnosis rules, as judged by the lead study doctor.
  • Have major problems on screening blood tests or an ECG, a test of the heart’s electrical activity.
  • Have a positive pregnancy test.
  • Have taken antibiotics within 2 weeks before joining.

Simplified for readability. The official criteria below are what the study team uses.

Official eligibility criteria

Inclusion Criteria: 1. Age ≥ 18 years 2. Be able to provide signed informed consent 3. Stated ability and willingness to comply with all study procedures 4. Able to take oral medications 5. Females of reproductive potential who are sexually active must be willing to use two of the following highly effective methods of contraception for the duration of study participation and for an additional 28 days after the end of study drug administration: barrier contraception (female condom, diaphragm, cervical cap with/without spermicide), hormonal contraception, or intrauterine device; OR one of the previously mentioned methods AND partner must use barrier contraception (male condom with/without spermicide) 6. Males of reproductive potential who are sexually active must be willing to use the following highly effective methods of contraception for the duration of study participation and for an additional 28 days after the end of study drug administration: barrier contraception (male condom with/without spermicide) AND partner must be postmenopausal, use hormonal contraception, have an intrauterine device, or use barrier contraception (female condom, diaphragm, cervical cap with/without spermicide) 7. Meet United Kingdom Parkinson's Disease Society Brain Bank Criteria: A. Diagnosis of a parkinsonism: * Bradykinesia, plus at least one of the following: * Muscular rigidity * 4-6 Hz resting tremor * Postural stability not caused by primary visual, vestibular, cerebellar or proprioceptive dysfunction B. At least three supportive criteria: * Unilateral onset of symptoms * Rest tremor * Progressive symptoms * Persistent asymmetry affecting the side of onset most * Excellent response to levodopa * Severe levodopa-induced chorea * Levodopa response for five years or more * Clinical course of 10 years or more 8. Fulfill the ROME IV Criteria for Functional Constipation, with a specific requirement that the patient must have three or fewer defecations per week (criterion Ai): * Must include two or more of the following: i. Three or fewer defecations per week ii. Straining during \> 25% of defecations iii. Lumpy or hard stools in \> 25% of defecations iv. Sensation of incomplete evacuation for \> 25% of defecations v. Sensation of anorectal obstruction/blockage for \> 25% of defecations vi. Manual maneuvers to facilitate \> 25% of defecations * Loose stools are rarely present without the use of laxatives * Insufficient criteria for irritable bowel syndrome * Criteria 1-3 must be fulfilled for at least three months with onset of symptoms at least six months prior to diagnosis Exclusion Criteria: 1. Diagnosis of atypical parkinsonism 2. Diagnosis of drug-induced parkinsonism 3. Diagnosis of vascular parkinsonism 4. Known allergy to pyridostigmine bromide or other study drug components 5. Current or recent (within 90 days of enrollment) use of pyridostigmine for any reason 6. History of any bowel surgery 7. History of bladder or bowel obstruction 8. Severe asthma or chronic obstructive pulmonary disease 9. Meet exclusion criteria noted in the UK Parkinson's Disease Society Brain Bank Criteria, at the PI's discretion: A.Exclusion of any of the following: * Repeated strokes with stepwise progression of parkinsonian features * Repeated head injury * Definite encephalitis * Oculogyric crises * Neuroleptic treatment at onset of symptoms * Greater than one affected relative * Sustained remission * Strictly unilateral features after 3 years * Supranuclear gaze palsy * Cerebellar signs * Early severe autonomic involvement * Early severe dementia * Babinski sign * Cerebral tumor or communicating hydrocephalus * Negative response to large doses of levodopa * 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine exposure 10. Significant abnormalities on laboratory analysis (complete blood count, comprehensive metabolic panel, thyroid stimulating hormone) conducted at the screening visit or within the three months prior if available for review 11. Significant abnormalities on screening electrocardiogram conducted at the screening visit or within the three months prior if available for review 12. Positive pregnancy test (if female of child-bearing age) 13. Antibiotic use within two weeks prior to enrollment

Study sites (1)

VT