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Clinic research of autologous platelets rich plasma promoting healing of Upper digestive tract ulcer

Clinic research of autologous platelets rich plasma promoting healing of Upper digestive tract ulcer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONN-15007573
Enrollment
Unknown
Registered
2015-12-14
Start date
2016-01-01
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

Upper digestive tract ulcer

Interventions

control group:Lansoprazole,30mg 1/day,(HP infection addition Livzon Weisanlian)
experimental group:Combined with autologous PRP on the basis of standard treatment on the patients of control group

Sponsors

Transfusion department of Southwest hospital Chongqing China
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients with upper gastrointestinal ulcer diagnosed by digestive endoscopy in Digestive System Department of our hospital; 2. Patients aged 18 to 60 (including 18 and 60 )years old, and gender not limited; 3. Patients without disease of hematopoietic system (blood routine inspection), and severe cardiopulmonary insufficiency (electrocardiogram and related symptoms); 4. Platelet count is more than 100*10^9/L; 5. Patients without Transfusion related diseases (AIDS, hepatitis c, hepatitis b, syphilis); 6. The patient or his legal representative signed on informed consent 7. Test result of pregnancy must be negative in women patient; 8. Patients can be cooperative on observation of curative effect and adverse reactions.

Exclusion criteria

Exclusion criteria: 1. Patients with aged younger than 18 years or older than 60 years, or with a definitive diagnosis of malignant ulcer ; 2. Patients with dysplasia of Hematopoietic system(blood routine inspection); 3. Platelet count is less than 100*10^9/L; 4. Patients with severe cardiopulmonary insufficiency (electrocardiogram and related symptoms); 5. Pregnancy or breast-feeding women; 6. Patients with any one of Transfusion related diseases (AIDS, hepatitis c, hepatitis b, syphilis); 7. The patient or his legal representative did not signe on informed consent; 8. Patients can not be cooperative on observation of curative effect and adverse reactions.

Design outcomes

Primary

MeasureTime frame
area of ulcer;

Countries

China

Contacts

Public ContactHua Lu
luhua678@sina.com+86 13132396892

Outcome results

None listed

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