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OncoMatch/Clinical Trials/NCT06775080

The Use of Propranolol in the Perioperative Period of Resectable Gastrointestinal Tumors

Is NCT06775080 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies propranolol (beta-blocker used treat high blood pressure) for gastrointestinal tumors.

Phase 2RecruitingHuashan HospitalNCT06775080Data as of Jun 2026Location: China

Treatment: propranolol (beta-blocker used treat high blood pressure)In this study, perioperative propranolol β-blockade was administered to patients with surgically resectable primary gastrointestinal tumors to explore the safety, efficacy, and alleviation of perioperative psychological stress. At the same time, a multi-omics study was conducted using clinical samples to explore the activation of anti-tumor immune response and its mechanism.

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Extracted eligibility criteria

Treatments studied

Other

propranolol (beta-blocker used treat high blood pressure)

Cancer type

Colorectal Cancer

Gastric Cancer

Hepatocellular Carcinoma

Pancreatic Cancer

Cholangiocarcinoma

Esophageal Carcinoma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≤ 65

Prior therapy

Cannot have received: surgery

Patients who have undergone surgery for GI tumors within the previous six months

Cannot have received: neoadjuvant chemotherapy

Patients receiving neoadjuvant chemotherapy prior to planned gastrointestinal tumor resection

Lab requirements

Kidney function

creatinine clearance ≤ 0.15 mmol/L

Liver function

AST or ALT or ALP ≤ 2.5x ULN, bilirubin ≤ 1.5x ULN

Cardiac function

Resting blood pressure > 100/60 mmHg, heart rate > 60 beats per minute; exclusion for pathological sinus node syndrome, sinus bradycardia (<60 bpm), AV block (any degree)

Resting blood pressure greater than 100/60mmHg, heart rate greater than 60 beats per minute. Pathological sinus node syndrome; Sinus bradycardia (less than 60 beats/minute); First, second or third degree AV block; Resting blood pressure less than 100/60 mmHg; Patients with renal insufficiency (defined as creatinine clearance greater than 0.15 mmol/L); Patients with hepatic insufficiency: AST or ALT or ALP > 2.5 times the upper limit of normal (ULN), bilirubin > 1.5 times the ULN

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT06775080 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior surgery, neoadjuvant chemotherapy disqualifies patients from enrollment.

Is there an age limit?

Yes. Patients must be 65 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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