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Optimization and Primary Clinical Application of Qilang Decoction Formulation

Optimization and Primary Clinical Application of Qilang Decoction Formulation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16009992
Enrollment
Unknown
Registered
2016-11-24
Start date
2017-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Chronic Functional Constipation

Interventions

treatment group:Particle simulation of Qilang + Lactulose Oral Solution agent
control group :Particle simulation of Qilang agent+Lactulose Oral Liquid

Sponsors

Shanghai Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) in line with the Rome IV functional constipation diagnostic criteria; 2) Aged 16 to 70 years old; 3) voluntarily join in this experiment, and sign the consent form.

Exclusion criteria

Exclusion criteria: 1) who did not meet the inclusion criteria, not required medication, can not determine the efficacy or incomplete information affect the efficacy or safety judgement; 2) after examination confirmed that the digestive tract tumors, or other systemic diseases involving the digestive tract, such as nerves, muscle lesions, as well as a clear cause of secondary constipation; 3) the age of 3 years old or older than 70 years of age or older: pregnancy or breast-feeding women; allergic constitution or a variety of drug allergy; 4) with heart, brain blood vessels, liver, kidney and hematopoietic system, such as severe primary disease, mental disease patients.

Design outcomes

Primary

MeasureTime frame
blood routine examination;routine urine test;blood biochemistry;Stool routine;electrocardiogram;

Countries

China

Contacts

Public ContactLi Yong

Shanghai Hospital of Traditional Chinese Medicine

liyong_sci@126.com+86 18116070688

Outcome results

None listed

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