Clinical trial · Interventional
The Use of Propranolol in the Perioperative Period of Resectable Gastrointestinal Tumors
The Use of Propranolol in the Perioperative Period of Resectable Gastrointestinal Tumors and the Study of Its Immune Mechanism Research
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Gastrointestinal Tumors | Digestive System Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| propranolol (beta-blocker used treat high blood pressure) | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- propranolol (beta-blocker used treat high blood pressure)+surgeries
- interventionNames
- Drug: propranolol (beta-blocker used treat high blood pressure)
Primary outcomes (13)
- measure
- Anxiety Depression Scale Scores
- timeFrame
- Within two years of enrollment
- description
- Hamilton Anxiety Scale. The higher the score, the worse the symptoms.
- measure
- heart rate
- timeFrame
- From enrollment to 24 days postoperatively
- description
- Sympathetic nervous system activation index
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 65 Years
Show eligibility criteria text
Inclusion Criteria: 1. Surgically resectable primary gastric cancer and colorectal cancer; 2. Age greater than 18 years old and less than 65 years old; 3. Negative pregnancy test for women of childbearing age; 4. ECOG score ≤2; 5. Signed informed consent. 6. Resting blood pressure greater than 100/60mmHg, heart rate greater than 60 beats per minute. Exclusion Criteria: 1\) Pregnant or breastfeeding women, or women with pregnancy plans within six months; 2) Patients with absolute or relative contraindications to propranolol: 1. Pathological sinus node syndrome; 2. Sinus bradycardia (less than 60 beats/minute); 3. First, second or third degree AV block; 4. Resting blood pressure less than 100/60 mmHg; 5. untreated pheochromocytoma; 6. untreated thyroid disease; 7. Patients on dihydropyridine or non-dihydropyridine calcium channel blockers (e.g., diltiazem, verapamil, nifedipine, amlodipine); 8. Severe peripheral vascular disease (intermittent claudication); 9. Patients on antiarrhythmic drugs (e.g., amiodarone, sotalol, digoxin); 10. Patients with renal insufficiency (defined as creatinine clearance greater than 0.15 mmol/L); 11. Patients with hepatic insufficiency: AST or ALT or ALP \> 2.5 times the upper limit of normal (ULN), bilirubin \> 1.5 times the ULN, ALP \> 2.5 12. Patients using colistin, digoxin, rizatriptan, cimetidine, hydralazine, guanethidine, or ergotamine. 13. Patients with a history of major depressive episodes; 3) Patients who have undergone surgery for GI tumors within the previous six months; 4) Patients receiving neoadjuvant chemotherapy prior to planned gastrointestinal tumor resection; 5) patients using conventional anxiolytic drugs (e.g. benzodiazepines), alpha-adrenergic agonists (e.g. colistin); 6) Patients using selective or non-selective β-adrenergic inhibitors (e.g., propranolol, metoprolol, atenolol, sotalol) within the last three months; 7) Patients with a history of stroke; 8) Patients with moderate or severe asthma, defined as requiring hospitalization or oral steroid therapy; (9) Those who, in the opinion of the physician, have other reasons for not being included in the treatment.
References
Publications (0)
Data not yet available