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A randomized controlled clinical study of platelet-rich plasma in the prevention of stricture after endoscopic submucosal dissection of large area early esophageal carcinoma

A randomized controlled clinical study of platelet-rich plasma in the prevention of stricture after endoscopic submucosal dissection of large area early esophageal carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051965
Enrollment
Unknown
Registered
2021-10-10
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Early esophageal cancer

Interventions

Experimental group :PRP was injected into the residual submucosa immediately after ESD, and acid-suppressing therapy was administered orally with prednyl acetate and PROTON pump inhibitor PPI for 8 w
Control group:Triamcinolone acetonide was injected into the residual submucosa immediately after ESD, and acid-suppressing therapy was administered orally with prednisoll acetate and PROTON pump inhib

Sponsors

The Affiliated Hospital of Southwest Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.It is considered to be early esophageal cancer by pathological examination or endoscopy, and the lesion area accounts for >=75% of the surrounding mucosa; the wound mucosal defect after ESD is >=75%; 2.Aged 18 to 80 years; 3.Good treatment compliance, can complete the follow-up; 4.No distant metastasis and surrounding invasion confirmed by imaging; 5.Patients and their families gave informed consent to this study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients with other malignant tumors or other esophageal diseases; 2.Complicated with organ dysfunction; 3.Poorly controlled diabetes, necrosis of the femoral head, peptic ulcer and tuberculosis; 4.Pregnant or lactating women; 5.Patients with contraindications to endoscopic surgery. Long-term oral administration of systemic cortisol hormones and anticoagulant and antiplatelet drugs.

Design outcomes

Secondary

MeasureTime frame
Incidence of postoperative complications;Glucocorticoid-related adverse events;

Primary

MeasureTime frame
Incidence of postoperative stenosis;Stooler score;Times of expansions;Duration of symptom remission;

Countries

China

Contacts

Public ContactShi Lei

The Affiliated Hospital of Southwest Medical University

Leishi@swmu.edu.cn+86 13982751821

Outcome results

None listed

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