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Clinical study of Shenling Baizhu Powder combined with Special Disease Prescription in the treatment of ulcerative colitis with dampness obstruction syndrome of spleen deficiency

Clinical study of Shenling Baizhu Powder combined with Special Disease Prescription in the treatment of ulcerative colitis with dampness obstruction syndrome of spleen deficiency

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006064
Enrollment
Unknown
Registered
2022-06-05
Start date
2022-06-05
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

ulcerative colitis

Interventions

The experimental group:Shenling Baizhu powder capsule combined with UC special prescription granules
The control group:Shenling Baizhu Powder placebo capsule combined with UC special prescription granules

Sponsors

Guangdong Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) 18-75 years old, male or female; (2) Meet the diagnostic criteria of ulcerative colitis; (3) Meet the criteria of mild and moderate active stage of ulcerative colitis; (4) Meet the criteria for waiting diagnosis of dampness obstruction syndrome of spleen deficiency; (5) The informed consent is signed.

Exclusion criteria

Exclusion criteria: (1) Chronic schistosomiasis, bacterial dysentery, intestinal tuberculosis and other infectious colitis, colonic Crohn's disease, radiation enteritis, ischemic enteritis; (2) Patients in lactation, pregnant women and intolerant to this drug; (3) patients with serious primary diseases such as heart, lung, liver, kidney and hematopoietic system, and mental illness; (4) Patients with serious complications such as local stenosis, toxic megacolon, intestinal obstruction, colon cancer, rectal cancer, intestinal perforation and anal diseases; (5) persons with disabilities defined by law (mute, deaf, blind, mental disorder, physical disability, intellectual disability). (6) Normal cognitive function, no dyslexia; Be able to actively cooperate and participate in investigation and research.

Design outcomes

Primary

MeasureTime frame
UC Disease activity index;

Secondary

MeasureTime frame
Blood sedimentation and CRP;Ibd Quality of life Questionnaire;Intestinal mucosa endoscopic and pathological scores;

Countries

China

Contacts

Public Contacthuangshaogang

Guangdong Provincial Hospital of Chinese Medicine

huangshaogang@gzucm.edu.cn13926451320

Outcome results

None listed

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