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The Effects of Two Induction Means on Emergence After General Anesthesia

NCT ID: NCT02974712

Last Updated: 2016-11-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-12-31

Study Completion Date

2017-03-31

Brief Summary

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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

Detailed Description

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Conditions

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Mean Arterial Pressure Heart Rate

Keywords

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Arterial blood gases MAP HR

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Fentanyl

After routine Induction, fentanyl was administrated.

Group Type EXPERIMENTAL

Fentanyl

Intervention Type DRUG

Saline

After routine Induction, same volume saline was administrated.

Group Type PLACEBO_COMPARATOR

Saline

Intervention Type DRUG

Interventions

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Fentanyl

Intervention Type DRUG

Saline

Intervention Type DRUG

Eligibility Criteria

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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.
Minimum Eligible Age

65 Years

Maximum Eligible Age

79 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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RenJi Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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20161114

Identifier Type: -

Identifier Source: org_study_id