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Premedication by Midazolam for Emergency Surgery

Primary Purpose

Anxiety

Status
Completed
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
placebo administration
midazolam intravenous administration
Sponsored by
University Hospital, Lille
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety focused on measuring premedication, preoperative anxiety, salivary cortisol level, anxiety visual analog scale

Eligibility Criteria

18 Years - 79 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • major patient undergoing elective surgery under general anesthesia with tracheal intubation
  • Anesthesia state 1 and 2
  • preoperative fasting for 6 hours
  • information and signed consent
  • social security
  • non pregnant women

Exclusion Criteria:

  • anesthesia state above 3
  • midazolam sensibility
  • pregnant or breastfeeding women
  • ICU patients
  • no consent
  • pediatric surgery
  • no social security
  • no tracheal intubation
  • required premedication in placebo group or midazolam sensibility in premedication group

Sites / Locations

  • Emergency, University Hopital

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Isotonic serum

Midazolam

Arm Description

placebo administration

midazolam intravenous administration 0.02mg/kg

Outcomes

Primary Outcome Measures

visual analog scale of anxiety
visual scale rated from 0 to 10 to describe the intensity of anxiety simple and reproducible measurement for a short period

Secondary Outcome Measures

salivary cortisol level
biologic measurement non-invasive, inexpensive and easy to perform. two determinations before and after premedication (at least 20 minutes)
Global anxiety
rated from 4 to 20 for global anxiety and from 2 to 10 for information request anxiety is high above 10 for women and 12 for men
Patient's satisfaction
rated from 1 for bad management to 5 for excellent management assessed at the output of the recovery room
Intraoperative consumption of hypnotics and opioids
Cumulative dose of hypnotics and opioids reduced to dose per kilogram
Comfort induction
rated from 1 for deep discomfort to 5 for good comfort
Intubation score
Rated from 1 bed conditions for intubation to 5 for excellent conditions
Adverse midazolam effects
assessed by variations of arterial pressure, heart rate, respiratory rate, oxygen saturation and end tidal of carbon dioxide for hemodynamics and respiratory adverse effects assessed by Observer's assessment of alertness/sedation for deep of sedation rated from 1 sleeping patient to 5 for awake patient
Output score of recovery room (Aldrete score)
rated from 0 to 10 essential for the output of recovery room

Full Information

First Posted
July 2, 2014
Last Updated
February 10, 2016
Sponsor
University Hospital, Lille
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1. Study Identification

Unique Protocol Identification Number
NCT02213302
Brief Title
Premedication by Midazolam for Emergency Surgery
Official Title
Effects of Premedication by Midazolam on Preoperative Anxiety for Emergency Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Completed
Study Start Date
July 2014 (undefined)
Primary Completion Date
January 2016 (Actual)
Study Completion Date
January 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Lille

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Preoperative anxiety is a subjective and painful experience and may have adverse psychological consequences and complicate anesthetic management. The aim of the study is to show the effect of premedication by midazolam on preoperative anxiety assessed by a visual analog scale and by measuring salivary cortisol levels. This study was a monocentric, prospective, blind randomized placebo controlled clinical study. Sixty patients, aged 18 to 79 years, to undergo elective surgery under general anesthesia with tracheal intubation must be enrolled and randomized to receive midazolam (0.02mg/kg) or placebo. The primary outcome is the reduction in anxiety assessed by a visual analog scale. The secondary outcomes are the reduction in salivary cortisol levels, the overall level of anxiety and the evaluation of respiratory and hemodynamic adverse effects of midazolam.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety
Keywords
premedication, preoperative anxiety, salivary cortisol level, anxiety visual analog scale

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
59 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Isotonic serum
Arm Type
Placebo Comparator
Arm Description
placebo administration
Arm Title
Midazolam
Arm Type
Active Comparator
Arm Description
midazolam intravenous administration 0.02mg/kg
Intervention Type
Drug
Intervention Name(s)
placebo administration
Other Intervention Name(s)
isotonic saline serum intravenous administration
Intervention Type
Drug
Intervention Name(s)
midazolam intravenous administration
Other Intervention Name(s)
hypnovel
Primary Outcome Measure Information:
Title
visual analog scale of anxiety
Description
visual scale rated from 0 to 10 to describe the intensity of anxiety simple and reproducible measurement for a short period
Time Frame
baseline, up to the end of support in recovery room
Secondary Outcome Measure Information:
Title
salivary cortisol level
Description
biologic measurement non-invasive, inexpensive and easy to perform. two determinations before and after premedication (at least 20 minutes)
Time Frame
baseline and at the entrance in operating room
Title
Global anxiety
Description
rated from 4 to 20 for global anxiety and from 2 to 10 for information request anxiety is high above 10 for women and 12 for men
Time Frame
baseline
Title
Patient's satisfaction
Description
rated from 1 for bad management to 5 for excellent management assessed at the output of the recovery room
Time Frame
at the end of the support in recovery room
Title
Intraoperative consumption of hypnotics and opioids
Description
Cumulative dose of hypnotics and opioids reduced to dose per kilogram
Time Frame
at anesthesia induction up to 10 minutes
Title
Comfort induction
Description
rated from 1 for deep discomfort to 5 for good comfort
Time Frame
at anesthesia induction
Title
Intubation score
Description
Rated from 1 bed conditions for intubation to 5 for excellent conditions
Time Frame
after intubation
Title
Adverse midazolam effects
Description
assessed by variations of arterial pressure, heart rate, respiratory rate, oxygen saturation and end tidal of carbon dioxide for hemodynamics and respiratory adverse effects assessed by Observer's assessment of alertness/sedation for deep of sedation rated from 1 sleeping patient to 5 for awake patient
Time Frame
baseline up to the end of support in recovery room
Title
Output score of recovery room (Aldrete score)
Description
rated from 0 to 10 essential for the output of recovery room
Time Frame
at the end of support in recovery room

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: major patient undergoing elective surgery under general anesthesia with tracheal intubation Anesthesia state 1 and 2 preoperative fasting for 6 hours information and signed consent social security non pregnant women Exclusion Criteria: anesthesia state above 3 midazolam sensibility pregnant or breastfeeding women ICU patients no consent pediatric surgery no social security no tracheal intubation required premedication in placebo group or midazolam sensibility in premedication group
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elise Blondé-Zoonekynd, Physician
Organizational Affiliation
University Hospital, Lille
Official's Role
Principal Investigator
Facility Information:
Facility Name
Emergency, University Hopital
City
Lille
ZIP/Postal Code
59000
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
18772216
Citation
Sun GC, Hsu MC, Chia YY, Chen PY, Shaw FZ. Effects of age and gender on intravenous midazolam premedication: a randomized double-blind study. Br J Anaesth. 2008 Nov;101(5):632-9. doi: 10.1093/bja/aen251. Epub 2008 Sep 4.
Results Reference
result
PubMed Identifier
2457102
Citation
Vogelsang J. The Visual Analog Scale: an accurate and sensitive method for self-reporting preoperative anxiety. J Post Anesth Nurs. 1988 Aug;3(4):235-9. No abstract available.
Results Reference
result
PubMed Identifier
15217656
Citation
Bauer KP, Dom PM, Ramirez AM, O'Flaherty JE. Preoperative intravenous midazolam: benefits beyond anxiolysis. J Clin Anesth. 2004 May;16(3):177-83. doi: 10.1016/j.jclinane.2003.07.003.
Results Reference
result
PubMed Identifier
16243241
Citation
Jerjes W, Jerjes WK, Swinson B, Kumar S, Leeson R, Wood PJ, Kattan M, Hopper C. Midazolam in the reduction of surgical stress: a randomized clinical trial. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005 Nov;100(5):564-70. doi: 10.1016/j.tripleo.2005.02.087.
Results Reference
result
PubMed Identifier
21602018
Citation
Wattier JM, Barreau O, Devos P, Prevost S, Vallet B, Lebuffe G. [Measure of preoperative anxiety and need for information with six issues]. Ann Fr Anesth Reanim. 2011 Jul-Aug;30(7-8):533-7. doi: 10.1016/j.annfar.2011.03.010. Epub 2011 May 23. French.
Results Reference
result
PubMed Identifier
8623940
Citation
Moerman N, van Dam FS, Muller MJ, Oosting H. The Amsterdam Preoperative Anxiety and Information Scale (APAIS). Anesth Analg. 1996 Mar;82(3):445-51. doi: 10.1097/00000539-199603000-00002.
Results Reference
result
PubMed Identifier
3156545
Citation
Reves JG, Fragen RJ, Vinik HR, Greenblatt DJ. Midazolam: pharmacology and uses. Anesthesiology. 1985 Mar;62(3):310-24.
Results Reference
result
PubMed Identifier
20224951
Citation
Zalunardo MP, Ivleva-Sauerborn A, Seifert B, Spahn DR. [Quality of premedication and patient satisfaction after premedication with midazolam, clonidine or placebo : Randomized double-blind study with age-adjusted dosage]. Anaesthesist. 2010 May;59(5):410-8. doi: 10.1007/s00101-010-1695-9. German.
Results Reference
result

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Premedication by Midazolam for Emergency Surgery

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