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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02974712
Other study ID # 20161114
Secondary ID
Status Not yet recruiting
Phase N/A
First received November 14, 2016
Last updated November 25, 2016
Start date December 2016
Est. completion date March 2017

Study information

Verified date November 2016
Source RenJi Hospital
Contact n/a
Is FDA regulated No
Health authority China: Ethics Committee
Study type Interventional

Clinical Trial Summary

This study aims to investigate the effects of different methods of administration on emergence period after laryngeal mask anesthesia in elderly patients undergoing transurethral endoscopic operation


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date March 2017
Est. primary completion date March 2017
Accepts healthy volunteers No
Gender Both
Age group 65 Years to 79 Years
Eligibility Inclusion Criteria:

- ASA level I or II,

- Aged from 65 to 79,

- With a duration of anesthesia <90 min.

Exclusion Criteria:

- Chronic obstructive pulmonary diseases (COPD),

- Severe heart disease,

- Difficult airway

- Liver and kidney dysfunction,

- Cerebrovascular disease,

- Bleeding volume >20 ml.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Drug:
Fentanyl

Saline


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
RenJi Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Mean arterial pressure (MAP) One hour after surgery No
Secondary Lengths of stays in the Post anesthesia care unit(PACU) One hour after surgery No
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