Study Results
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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UNKNOWN
35 participants
OBSERVATIONAL
2021-10-20
2023-05-01
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Group ANI
No interventions assigned to this group
Group Control
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients who underwent gynecological surgery under general anesthesia, who underwent erector spina block, and whose pain was followed by analgesia nociception index or conventional methods for intraoperative pain monitoring
* Patients whose informed consent was read and consent was obtained from them and their guardians
Exclusion Criteria
* central-autonomic nervous system disease
* neuropsychiatric disease
* receiving opioid therapy
* Use of drugs that will affect cardiac autonomic regulation
* Known allergy to the drugs to be applied
* Contraindicated for ESP block
* Patients who do not agree to participate in the study will not be included in the study.
* Patients who were administered drugs to stabilize the patient's hemodynamics during the operation
18 Years
65 Years
FEMALE
Yes
Sponsors
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Zeynep Koc
UNKNOWN
Zonguldak Bulent Ecevit University
OTHER
Responsible Party
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Çağdaş Baytar
assistant professor
Locations
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Zonguldak Bülent Ecevit University Medicine Faculty
Zonguldak, Kozlu, Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Murat Can, prof.dr
Role: primary
References
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Koc Z, Baytar C, Bollucuoglu K, Koksal BG, Okyay RD, Piskin O, Ayoglu H. Intraoperative analgesia management by monitoring the analgesia nociception index in gynecological surgeries involving erector spinae plane block: a randomized controlled study. J Clin Monit Comput. 2025 Jul 15. doi: 10.1007/s10877-025-01330-x. Online ahead of print.
Other Identifiers
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2021/18-4
Identifier Type: -
Identifier Source: org_study_id