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Clinical Trials/CTRI/2015/01/005470
CTRI/2015/01/005470Recruiting未知

A non-interventional, cross-sectional, clinico-epidemiological study to determine the prevalence of clinical Subtypes of Constipation in INdian patients - The SCIoN Study

Abbott India Limited0 sites920 target enrollmentStarted: TBDLast updated:
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Trial Snapshot

Phase
未知
Status
Recruiting
Enrollment
920
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Inclusion Criteria

  • •1.Patients of either sex, aged 18 years and above.
  • •2.Patients who have symptoms related to constipation (criteria for functional constipation and IBS-C fulfilled for the last 3 months with symptom onset at least 6 months prior to inclusion into the study)
  • •3.Patients willing to sign the patient authorization form.

Exclusion Criteria

  • •1.Pregnant or lactating women.
  • •2.Patients with intestinal obstruction (known or suspected).
  • •3.Patients with any disease with the potential to precipitate intestinal obstruction.
  • •4.Patients with acute abdomen (sudden, severe abdominal pain of unclear etiology).

Investigators

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