A Trial of Docusate Sodium and Sorbitol Rectal Solution for the in Patients With Constipation

Ferring

Status and phase

Completed

Phase 3

Conditions

Constipation

Treatments

Drug: Glycerine

Drug: Docusate sodium and sorbitol rectal solution

Study type

Interventional

Funder types

Industry

Identifiers

NCT01474499

FE999306 CS01

Details and patient eligibility

About

This study aims to evaluate the efficacy and safety of the docusate sodium and sorbitol rectal solution produced by Ferring Pharmaceutical (China) Ltd. in treating Chinese patients with constipation.

Enrollment

300 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Have signed the informed consent form and have been verbally told of the details of the trial and treatment procedures
Is a citizen of the People's Republic of China
Males and females aged between 18 and 65 years inclusive
A history of constipation symptoms for at least 6 months, with occurrence of two or more of the symptoms during the 3 months before screening:
1. More than 1/4 of stool classifiable as Type I or Type II on the Bristol Stool Scale;
2. Sensation of incomplete evacuation at least 1/4 of the time;
3. Straining during defecation at least 1/4 of the time;
4. Sensation of ano-rectal blockage or obstruction during defecation at least 1/4 of the time;
5. Manual manoeuvres needed often to facilitate defecations (e.g. digital evacuation) at least 1/4 of the time;
6. Fewer than 3 bowel movements per week
No bowel movement within two days prior to randomisation

Exclusion criteria

Patients who are suspected to have colorectal cancer;
Patients showing signs of bleeding in the digestive tract or inflammatory bowel disease;
Patients experiencing abdominal discomfort or intestinal blockage for which the cause has yet to be determined;
Patients allergic to docusate or sorbitol;
Patients allergic to glycerine;
Those pregnant, breastfeeding, or with the intention of becoming pregnant, or fertile women who are not on effective birth control（i.e. an IUD (intrauterine device), oral contraceptives or other obstructive measures;
Severe liver damage (ALT (alanine aminotransferase), AST (aspartate transaminase), TBIL (serum total bilirubin) more than 2 times the upper limit of normal)
Kidney function impairment (Cr (creatinine clearance rate), BUN (blood urea nitrogen) more than 1.5 times the upper limit of normal)
Patients who have participated in any other clinical trial during the last 3 months;
Diabetics who are currently undergoing insulin treatment;
Patients who are unable to suspend using treatments that affect the kinetics of the digestive system in the 5 days prior randomisation. Such treatments include prokinetic drugs, erythromycin analogues, laxatives, etc;
Other patient factor(s) (e.g. medical history, concurrent illness(es), laboratory test result(s), etc.) at Screening that in the opinion of the investigator(s) would put the trial patient at excessive risk;
Patients who are unable to act in a legal capacity, unable to meet or perform study requirements, or are known or suspected as unable to comply with the study protocol.