Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:11 AM
Ignite Modification Date:
2025-12-25 @ 4:11 AM
NCT ID:
NCT03523520
Eligibility Criteria:
Inclusion Criteria:
* Complaint of opioid-induced constipation refractory to other therapy (enemas, laxatives, stool softeners)
* Ageā„18y/o
* Not pregnant or lactating (negative urinary pregnancy test)
* No contraindication to Methylnaltrexone or Naloxegol
Exclusion Criteria:
* Age\<18y/o
* Pregnancy or lactation
* Contraindication to Methylnaltrexone or Naloxegol
* Assigned NPO
* Small bowel obstruction
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03523520
Study Brief:
Protocol Section:
NCT03523520