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Comparison of the efficacy of linalopone and lactose in the treatment of constipation-type irritable bowel syndrome

Comparison of the efficacy of linalopone and lactose in the treatment of constipation-type irritable bowel syndrome

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050993
Enrollment
Unknown
Registered
2021-09-10
Start date
2021-09-30
Completion date
Unknown
Last updated
2022-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

constipation-type irritable bowel syndrome

Interventions

Experimental group:Lenalopeptides

Sponsors

Tongliang Hospital, the First Affiliated Hospital of Chongqing Medical University (Chongqing Tongliang District People's Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years; 2. Diagnosed as IBS-C according to Rome IV diagnostic criteria; 3. Colonoscopy has been performed in the past 2 years to exclude intestinal organic lesions (tumor, inflammatory lesions, etc.); 4. Voluntarily accept the research plan, accept the review and follow-up on time, and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant and lactating patients, or patients planning to have children during the study period; 2. Suffering from organic diseases that may cause constipation: such as metabolic diseases (diabetes, hypothyroidism, parathyroid disease, etc.), neurogenic diseases (Parkinson's, brain tumor, multiple sclerosis, etc.), primary colon diseases (intestinal tumors, intestinal inflammation, rectal and anal lesions, etc.); 3. Drug-induced constipation: mainly includes constipation induced by anticholinergic drugs, opioids, calcium antagonists, antidepressants, antihistamines, antispasmodics, anticonvulsants, etc.; 4. Suffering from diseases that affect the development or results of the trial: such as mental illness, gastrointestinal bleeding, intestinal obstruction, severe cardiopulmonary disease, digestive system tumors or history of gastrointestinal surgery, etc.; 5. Those who are allergic to the drugs used in this study; 6. Those who have taken drugs that affect intestinal function in the past 2 weeks.

Design outcomes

Primary

MeasureTime frame
abdominal pain score;number of total voluntary defecation per week;

Secondary

MeasureTime frame
symptoms indicators;irritable bowel syndrome symptom severity score;evaluation scale based on the reported clinical outcomes of patients with chronic gastrointestinal disease;hospital anxiety and depression scale;untoward effect;

Countries

China

Contacts

Public ContactZeng Guli

Tongliang Hospital, the First Affiliated Hospital of Chongqing Medical University (Chongqing Tongliang District People's Hospital)

705620824@qq.com+86 13996360924

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026