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The effect of pre-administate of antiemetics on the ED50 of norepinephrine in the prevention of hypotension during induction period in elderly patients elective laparoscopic gastrectomyor intestinal resection

The effect of pre-administate of antiemetics on the ED50 of norepinephrine in the prevention of hypotension during induction period in elderly patients elective laparoscopic gastrectomyor intestinal resection

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061900
Enrollment
Unknown
Registered
2022-07-09
Start date
2022-07-20
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Stomach tumor, colon, rectal tumor

Interventions

Test group:Granisetron

Sponsors

Sir Run Run Shaw Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 74 Years

Inclusion criteria

Inclusion criteria: 1. Elderly patients with ASA class I or II; 2. Aged 60-74 years (the population at this stage is defined as young old people by WHO); 3. 18.5 <= BMI <= 23.9; 4. The patient was diagnosed with gastric or intestinal tumor at Run Run Shaw Hospital and underwent laparoscopic gastric or intestinal resection as scheduled; 5. Patients with one or more high-risk factors for postoperative nausea and vomiting (PONV); 6. Voluntarily participate in this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Severe history of cardiovascular and cerebrovascular diseases; 2. Patients with a history of severe arrhythmia, cardiac insufficiency, or severe heart valve disease; 3. history of serious respiratory diseases; 4. Hypertensive patients taking ACEI or ARB for a long time or patients with secondary hypertension or above; 5. Hyperthyroidism; 6. Liver and kidney insufficiency; 7. Untreated hyperglycemia or those with poor treatment effect; 8. Patients who are allergic to anesthetics (such as propofol and cisatracurium besylate); 9. Gastrointestinal obstruction, allergic to granisetron or related compounds; 10. Vulnerable groups, including mentally ill, critically ill patients, cognitively impaired, pregnant women, illiterate, etc.

Design outcomes

Primary

MeasureTime frame
mean arterial pressure;Blood pressure;heart rate;Entropy index;oxygen saturation;end-tidal carbon dioxide;

Secondary

MeasureTime frame
urine output;Infusion volume;

Countries

China

Contacts

Public ContactGang Chen

Sir Run Run Shaw Hospital, Zhejiang University School of Medicine

chengang120@hotmail.com+86 13757118681

Outcome results

None listed

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