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Using Preoperative Anxiety Score to Determine the Total Dose of Butorphanol for Sedation

Primary Purpose

Preoperative Anxiety Score, Total Dose of Butorphanol

Status
Completed
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Butorphanol
physiological saline
Sponsored by
Shengjing Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Preoperative Anxiety Score focused on measuring Butorphanol, preoperative anxiety, sedation, recommend dose

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • American Society of Anesthesiologists (ASA)Ⅰ-Ⅱ
  • 18-75 years
  • Scheduled for elective low limb orthopaedic procedures under spinal anesthesia

Exclusion Criteria:

  • central system disease
  • cardiovascular disease
  • autonomic nervous system disease
  • long term use of analgesic, sedative, and anti-anxiety drugs
  • psychosis
  • a patient with a language communication disorder not willing to cooperate with the experimenter

Sites / Locations

  • shengjing hospital of China medical university

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Placebo Comparator

Experimental

Placebo Comparator

Arm Label

preoperative anxiety and butorphanol

preoperative anxiety and saline

non-preoperative anxiety and butorphanol

non-preoperative anxiety and saline

Arm Description

preoperative anxiety scores of patients in Group A were >11 and received an intravenous loading dose of 15ug/kg butorphanol 5 min before starting the surgery, then followed by infusion of 7.5ug/kg/h butorphanol and stopped infusion until the Ramsay sedation score reached 4 points

preoperative anxiety scores of patients in Group B were >11 and received an infusion of the same volume of physiological saline

preoperative anxiety scores of patients in Group C were ≤ 11 and received an intravenous loading dose of 15ug/kg butorphanol 5 min before starting the surgery, then followed by infusion of 7.5ug/kg/h butorphanol and stopped infusion until the Ramsay sedation score reached 4 points

preoperative anxiety scores of patients in Group D were ≤11 and received an infusion of the same volume of physiological saline

Outcomes

Primary Outcome Measures

preoperative anxiety score (Amsterdam preoperative anxiety and information scale, APAIS)
evaluate the preoperative anxiety score one day before the surgery, the scale ranges from 0-33. And we define a score of 11 as a cut-off point, the higher the score the more serious the preoperative anxiety is
Ramsay sedation score (Ramsay sedation scale, RSS)
evaluate the Ramsay sedation score 10 min after getting into the operation room and 5, 10, 15, 30min after infusion. The Ramsay sedation scale ranges from 1-6. 1, anxious and agitated or restless or both; 2, cooperative, orientated, and tranquil; 3, responds to commands only; 4, brisk response to a light glabellar tap or auditory stimulus; 5, sluggish response to a light glabellar tap or auditory stimulus; and 6, no response to a light glabellar tap or auditory stimulus. A sedative state with RSS 4 was considered as an adequate level of sedation
the time when Ramsay sedation score reached 4 points
record the time when Ramsay sedation score reached 4 points. The Ramsay sedation scale ranges from 1-6. 1, anxious and agitated or restless or both; 2, cooperative, orientated, and tranquil; 3, responds to commands only; 4, brisk response to a light glabellar tap or auditory stimulus; 5, sluggish response to a light glabellar tap or auditory stimulus; and 6, no response to a light glabellar tap or auditory stimulus. A sedative state with RSS 4 was considered as an adequate level of sedation

Secondary Outcome Measures

vital signs
Record Mean Arterial Pressure(MAP)10 min after getting into the operation room and 5, 10, 15, 30min after infusion
The incidence of nausea/ vomiting, dizzy, bradycardia and hypotension
Investigate the incidence of nausea/ vomiting, dizzy, bradycardia and hypotension in the first day after the surgery
post-operative visual analgesia scale scores (VAS)
investigate the VAS every hour till 6 hours and then every 2 hours till 24 hours. The VAS ranges from 1-10. 0 means painless; 1-3 means mild pain; 4-6 means moderate pain and 7-10 means severe pain
Vital signs
Record Spo2 10 min after getting into the operation room and 5, 10, 15, 30min after infusion
Vital signs
Record Heart Rate(HR) 10 min after getting into the operation room and 5, 10, 15, 30min after infusion

Full Information

First Posted
January 13, 2019
Last Updated
January 17, 2019
Sponsor
Shengjing Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03810391
Brief Title
Using Preoperative Anxiety Score to Determine the Total Dose of Butorphanol for Sedation
Official Title
Using Preoperative Anxiety Score to Determine the Total Dose of Butorphanol for Sedation in Patients Undergoing Lower Limb Orthopedic Procedures: A Randomized, Double-blind, Placebo-controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
December 1, 2017 (Actual)
Primary Completion Date
December 20, 2018 (Actual)
Study Completion Date
December 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shengjing Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Orthopedic surgeries are considered to be discomfortable and the sense of fear and anxiety of patients who already have preoperative anxiety may be aggravated by intraoperative stimulation, which may contribute to postoperative complications. Previous studies have found that high anxiety predicts increased sedative requirements. Therefore, the investigators explored the relationship between anxiety and intraoperative butorphanol requirements and the investigators evaluated the specific sedative requirement which can keep satisfactory sedative state for patients by preoperative anxiety score
Detailed Description
A total of one hundred and eighteen patients who were to undergoing lower limb orthopedic procedures with spinal anesthesia were selected,the Amsterdam preoperative anxiety and information scale was used to evaluated the degree of preoperative anxiety one day before the surgery. Patients in preoperative anxiety group were randomly allocated to two groups: butorphanol group (Group A) and physiological saline group (Group B); Patients in non-preoperative anxiety group were also randomly allocated to two groups: butorphanol group (Group C) and physiological saline group (Group D). In Group A and Group C, patients received an intravenous loading dose of 15ug/kg butorphanol 5 min before starting the surgery, then followed by infusion of 7.5ug/kg/h butorphanol and stopped infusion until the Ramsay sedation score reached 4 points, Group B and Group D received an infusion of the same volume of physiological saline. The sedation scores were recorded 10 min after getting into the operation room and 5, 10, 15, 30min after infusion of butorphanol or physiological saline. The duration when Ramsay sedation score reached 4 points in Group A and C, adverse events and post-operative visual analgesia scale scores were also recorded and compared.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preoperative Anxiety Score, Total Dose of Butorphanol
Keywords
Butorphanol, preoperative anxiety, sedation, recommend dose

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
the Amsterdam preoperative anxiety and information scale was used to evaluated the degree of preoperative anxiety one day before the surgery. Patients in preoperative anxiety group were randomly allocated to two groups: butorphanol group (Group A) and physiological saline group (Group B); Patients in non-preoperative anxiety group were also randomly allocated to two groups: butorphanol group (Group C) and physiological saline group (Group D) In Group A and Group C, patients received an intravenous loading dose of 15ug/kg butorphanol 5 mins before starting the surgery, then followed by infusion of 7.5ug/kg/h butorphanol and stopped infusion when the Ramsay sedation score (RSS) reached 4 , Group B and Group D received an infusion of the same volume of physiological saline
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
126 (Actual)

8. Arms, Groups, and Interventions

Arm Title
preoperative anxiety and butorphanol
Arm Type
Experimental
Arm Description
preoperative anxiety scores of patients in Group A were >11 and received an intravenous loading dose of 15ug/kg butorphanol 5 min before starting the surgery, then followed by infusion of 7.5ug/kg/h butorphanol and stopped infusion until the Ramsay sedation score reached 4 points
Arm Title
preoperative anxiety and saline
Arm Type
Placebo Comparator
Arm Description
preoperative anxiety scores of patients in Group B were >11 and received an infusion of the same volume of physiological saline
Arm Title
non-preoperative anxiety and butorphanol
Arm Type
Experimental
Arm Description
preoperative anxiety scores of patients in Group C were ≤ 11 and received an intravenous loading dose of 15ug/kg butorphanol 5 min before starting the surgery, then followed by infusion of 7.5ug/kg/h butorphanol and stopped infusion until the Ramsay sedation score reached 4 points
Arm Title
non-preoperative anxiety and saline
Arm Type
Placebo Comparator
Arm Description
preoperative anxiety scores of patients in Group D were ≤11 and received an infusion of the same volume of physiological saline
Intervention Type
Drug
Intervention Name(s)
Butorphanol
Other Intervention Name(s)
butorphanol tartrate injection
Intervention Description
intravenous loading dose of 15ug/kg butorphanol,and followed by infusion of 7.5ug/kg/h butorphanol and stopped infusion until the Ramsay sedation score reached 4 points
Intervention Type
Other
Intervention Name(s)
physiological saline
Intervention Description
intravenous infusion of the same volume of physiological saline
Primary Outcome Measure Information:
Title
preoperative anxiety score (Amsterdam preoperative anxiety and information scale, APAIS)
Description
evaluate the preoperative anxiety score one day before the surgery, the scale ranges from 0-33. And we define a score of 11 as a cut-off point, the higher the score the more serious the preoperative anxiety is
Time Frame
one day before the surgery
Title
Ramsay sedation score (Ramsay sedation scale, RSS)
Description
evaluate the Ramsay sedation score 10 min after getting into the operation room and 5, 10, 15, 30min after infusion. The Ramsay sedation scale ranges from 1-6. 1, anxious and agitated or restless or both; 2, cooperative, orientated, and tranquil; 3, responds to commands only; 4, brisk response to a light glabellar tap or auditory stimulus; 5, sluggish response to a light glabellar tap or auditory stimulus; and 6, no response to a light glabellar tap or auditory stimulus. A sedative state with RSS 4 was considered as an adequate level of sedation
Time Frame
during the surgery
Title
the time when Ramsay sedation score reached 4 points
Description
record the time when Ramsay sedation score reached 4 points. The Ramsay sedation scale ranges from 1-6. 1, anxious and agitated or restless or both; 2, cooperative, orientated, and tranquil; 3, responds to commands only; 4, brisk response to a light glabellar tap or auditory stimulus; 5, sluggish response to a light glabellar tap or auditory stimulus; and 6, no response to a light glabellar tap or auditory stimulus. A sedative state with RSS 4 was considered as an adequate level of sedation
Time Frame
Ramsay sedation score reach 4 points during the surgery
Secondary Outcome Measure Information:
Title
vital signs
Description
Record Mean Arterial Pressure(MAP)10 min after getting into the operation room and 5, 10, 15, 30min after infusion
Time Frame
during the surgery
Title
The incidence of nausea/ vomiting, dizzy, bradycardia and hypotension
Description
Investigate the incidence of nausea/ vomiting, dizzy, bradycardia and hypotension in the first day after the surgery
Time Frame
in the first day after the surgery
Title
post-operative visual analgesia scale scores (VAS)
Description
investigate the VAS every hour till 6 hours and then every 2 hours till 24 hours. The VAS ranges from 1-10. 0 means painless; 1-3 means mild pain; 4-6 means moderate pain and 7-10 means severe pain
Time Frame
within 24 hours after the surgery
Title
Vital signs
Description
Record Spo2 10 min after getting into the operation room and 5, 10, 15, 30min after infusion
Time Frame
during the surgery
Title
Vital signs
Description
Record Heart Rate(HR) 10 min after getting into the operation room and 5, 10, 15, 30min after infusion
Time Frame
during the surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: American Society of Anesthesiologists (ASA)Ⅰ-Ⅱ 18-75 years Scheduled for elective low limb orthopaedic procedures under spinal anesthesia Exclusion Criteria: central system disease cardiovascular disease autonomic nervous system disease long term use of analgesic, sedative, and anti-anxiety drugs psychosis a patient with a language communication disorder not willing to cooperate with the experimenter
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Junchao Zhu, professor
Organizational Affiliation
Shengjing Hospital
Official's Role
Study Director
Facility Information:
Facility Name
shengjing hospital of China medical university
City
Shenyang
State/Province
Liao Ning
ZIP/Postal Code
110004
Country
China

12. IPD Sharing Statement

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Using Preoperative Anxiety Score to Determine the Total Dose of Butorphanol for Sedation

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