Intranasal Sedation With Dexmedetomidine

Sponsor
University Medical Centre Ljubljana (Other)
Overall Status
Unknown status
CT.gov ID
NCT03251222
Collaborator
(none)
40
1
2
13.9
2.9

Study Details

Study Description

Brief Summary

For patients with eye surgery and shorter surgery, sedation is a well-established method in preserved consciousness and has been successfully used for several years. We have also developed and published a valid protocol (1).

Remifentanil is used in intravenous infusion for sedation and anxiolysis. Remifentanil is a descriptive analgesic, which also works partially anxiolytically. In eye surgery, it is important that the patient cooperates during the operation and should not be ashamed, as injury to the eye could occur, because the vitrectomes are performed with a fine intraocular endoscopic technique, in which the operator inserts his instruments through the whiteness into the eye. For this reason, we have not yet added additional sedatives (for example, midazolam), which is very unpredictable as regards sedation. Remifentanil is also very unpredictable and it is very difficult to control it during the operation so that the patient is saturated with satisfaction.

Lately, dexmedetomidine has been successfully used in sedation for other areas of surgery (eg neurosurgery, maxillofacial surgery, ORL). It is a safe, proven, active substance with alpha 2 agonistic effect, which has not yet been used in the field of ocular surgery and has not yet published articles in this field. The substance is very suitable because it works mildly sedative and at the same time analgesic.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

For patients with eye surgery and shorter surgery, sedation is a well-established method in preserved consciousness and has been successfully used for several years. We have also developed and published a valid protocol (1).

Remifentanil is currently used for intravenous infusion for analgesia and anxiolysis. Remifentanil is an opioid analgesic, which also works partially anxiolytically. It has been studied in detail for postnatal analgesia (2). In eye surgery, it is important that the patient cooperates during the operation and should not be ashamed, as injury to the eye could occur, because the vitrectomes are performed with a fine intraocular endoscopic technique, in which the operator inserts his instruments through the whiteness into the eye. For this reason, we have not yet added additional sedatives (for example, midazolam), which is very unpredictable and a rapidly shallow sedation can pass into the deeper. Remifentanil is also very unpredictable and it is very difficult to control it during the operation, so that the patient is satisfactorily analgesized at all times, but still co-operable.

Recently, dexmedetomidine (3-5) has been successfully used in other areas of surgery (eg neurosurgery, maxillofacial surgery, ORL) and intensive sedation therapies. It is a safe, proven, active substance with alpha 2 agonistic effect, which has not yet been used in the field of ocular surgery and has not yet published articles in this field. The substance is very suitable because it works mildly sedative and at the same time analgesic (3).

Dexmedetomidine is predominantly administered intravenously, and intranasal administration (6-8) has also been established in pediatric patients.

We decided to use intranasal use because it is simple, safe and suitable for such treatments because intravenous dexmedetomidine could not be administered because it should be given enough time before surgery (at least 40 min) because otherwise the appropriate effect . Patients for such operations will enter the operating room directly from the departments on foot and dexmedetomidine could not be started earlier, as it is not possible to provide adequate control in the department. A sedentary patient would also not be able to walk into an operational one, which would greatly complicate and also increase logistics.

The study is applicable, as it will provide objective indicators, which type of sedation is most effective and safe for vitreoretinal interventions.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Intranasal Sedation With Dexmedetomidine for Vitroretinal Procedures
Actual Study Start Date :
Jan 1, 2017
Anticipated Primary Completion Date :
Dec 1, 2017
Anticipated Study Completion Date :
Mar 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Dexmedetomidine group

Patients who will receive Dexmedetomidine intranasal prior the sedation with remifentanil

Drug: Dexmedetomidine
Intranasal aplication of dexmedetomidine

Placebo Comparator: Placebo Concentrate

Patients will recive 0.9% NaCl

Other: Placebo - Concentrate
Intranasal aplication of 0.9% NaCl
Other Names:
  • Placebo
  • Outcome Measures

    Primary Outcome Measures

    1. remifentanil consuption [duration of the procedure]

      the consuption of remifentanil requiered to reach the appropriate sedation will be meassured

    Secondary Outcome Measures

    1. Oxigen Saturation [duration of the procedure]

      Oxigen Saturation measured with pulse oxymetry

    Other Outcome Measures

    1. BIS- bispectral index [duration of the procedure]

      Depth of the sedation

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes

    Inclusion Criteria: patients who will be operated on the eye (vitreoretinal interventions) patients with ASA status 1-3

    -

    Exclusion Criteria:
    • patients who will not want to be operated in the sedation but in general anesthesia

    • poor general condition (ASA> 3)

    • with severe cardiac disease (NYHA> 3)

    • with severe pulmonary obstructive disease (FEV1 <40%)

    • neurological diseases

    • psychiatric patients

    • patients receiving regular psychotropic treatment

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 UMCLjubljana, CD of Anaesthesiology and Intensive Therapy Ljubljana Slovenia 1000

    Sponsors and Collaborators

    • University Medical Centre Ljubljana

    Investigators

    • Study Chair: Vesna Novak-Jankovic, PROF, UMCLjubljana, KOAIT

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Iztok Potocnik, M.D., PHD, University Medical Centre Ljubljana
    ClinicalTrials.gov Identifier:
    NCT03251222
    Other Study ID Numbers:
    • UKC-OCKL1
    First Posted:
    Aug 16, 2017
    Last Update Posted:
    Aug 16, 2017
    Last Verified:
    Aug 1, 2017
    Keywords provided by Iztok Potocnik, M.D., PHD, University Medical Centre Ljubljana
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 16, 2017