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

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-65
SponsorHuashan Hospital

About this trial

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.

Eligibility criteria

Qualifiers

Surgically resectable primary gastric cancer and colorectal cancer;

Age greater than 18 years old and less than 65 years old;

Negative pregnancy test for women of childbearing age;

ECOG score ≤2;

Disqualifiers

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;

Trial design

Treatments tested in this trial

  • propranolol (beta-blocker used treat high blood pressure)

Treatment groups

40 Participants
are divided into 1 treatment group

Sponsors and collaborators