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The effect of propofol combined with intravenous lidocaine on elderly colonoscopy: a randomized, controlled, double-blind study

The effect of propofol combined with intravenous lidocaine on elderly colonoscopy: a randomized, controlled, double-blind study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021818
Enrollment
Unknown
Registered
2019-03-11
Start date
2019-05-01
Completion date
Unknown
Last updated
2019-03-18

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

Conditions

Colon disease

Interventions

Control group:Normal saline

Sponsors

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) aged = 65 years old; (2) ASA grade I or II; (3) colonoscopy; (4) signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with known cardiopulmonary function insufficiency; severe cardiovascular disease history (eg, heart failure, severe arrhythmia, etc.); family history of Adams-Stokes syndrome; unstable angina, or patients with myocardial infarction within 6 months; tachycardia/slow history requiring medication and/or resting ECG heart rate 160mmHg and/or diastolic blood pressure >100mmHg after antihypertensive treatment; (3) Craniocerebral injury, possible intracranial hypertension, cerebral artery tumor, cerebrovascular accident history; schizophrenia, mania, insanity, long-term use of psychotropic drugs, history of cognitive dysfunction, or screening MMSE unqualified suggestive of cognitive dysfunction; (4) Respiratory function insufficiency, history of obstructive pulmonary disease, history of asthma, wheezing or sleep apnea syndrome, or history of bronchospasm requiring treatment within 3 months prior to screening or upper respiratory tract infection 1 week before screening, fever, asthma; (5) Have a history of malignant hyperthermia or family history; (6) Have a clinically significant history of abnormal liver, kidney, blood system or metabolic system; (7) Have a history of colectomy; (8) Those with severe infection, trauma or major surgery 4 weeks before screening; or delayed gastric emptying and acute gastrointestinal bleeding; (9) Patients with known hyperalgesia or dysalgesia or refractory cancer pain; (10) Patients with a central nervous system disorder or mental disorder which meet the DSM diagnostic criteria; (11) A patient who is contraindicated to intravenous general anesthesia.

Design outcomes

Primary

MeasureTime frame
Propofol dosage;abdominal pain VAS score;

Secondary

MeasureTime frame
Hemodynamics;

Countries

China

Contacts

Public ContactWangning Shangguan

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University

sgwning@163.com+86 13587637891

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 18, 2026