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Celecoxib for prevention of esophageal stricture after endoscopic treatment in early esophageal cancer/ precancerous lesion: a clinical randomized controlled trial

Celecoxib for prevention of esophageal stricture after endoscopic treatment in early esophageal cancer/ precancerous lesion: a clinical randomized controlled trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14005085
Enrollment
Unknown
Registered
2014-08-06
Start date
2014-08-06
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

early esophageal cancer/ precancerous lesion

Interventions

treatment group:endoscopic treatment+Celecoxib(200mg bid*7 days preoperative+200mg qd*3 months postoperative)
control group:endoscopic treatment

Sponsors

Department of Gastroenterology, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Pathology confirmed high-grade intraepithelial neoplasia or mucosa cancer of esophageal mucosa; (2) The scope of lesions involving more than 1/2 of the lumen circumference; (3) Endoscopic classification of I, IIa and IIb, IIc type; (4) Lesion invasion less than submucosa without lymph node metastasis identified by endoscopic ultrasonography and chest enhancement CT scan; (5) No obvious heart or lung dysfunction; (6) No blood coagulation disorders.

Exclusion criteria

Exclusion criteria: (1) Inability of resecting en bloc or tumor invasion of muscularis propria or serosa identified by postoperative pathology; (2) Lymph node invasion or local/distant metastasis; (3) History of malignant tumors; (4) Sulphonamide allergy; (5) Severe heart of pulmonary disease; (6) Dysfunction of liver or kidney; (7) Perinatal and nursing mothers; (8) Other NSAIDs using before trail inclusion; (9) Additional postoperative surgery, chemotherapy or radiotherapy; (10) Active peptic ulcer/bleeding; (11) Severe heart failure.

Design outcomes

Primary

MeasureTime frame
Esophageal stricture rate;

Secondary

MeasureTime frame
dysphagia scoring;Balloon dilation time;

Countries

China

Contacts

Public ContactHu Bing
hubingnj@163.com+86 18980601278

Outcome results

None listed

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