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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03217292
Other study ID # 2011-KAEK-25 2016/13-06
Secondary ID
Status Completed
Phase N/A
First received July 2, 2017
Last updated July 13, 2017
Start date July 1, 2016
Est. completion date December 1, 2016

Study information

Verified date July 2017
Source Bursa Yüksek Ihtisas Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Analgesia following video-assisted thoracoscopic surgery (VATS) is important for the prevention of postoperative pulmonary complications.Various regional methods of anesthesia are currently being used to achieve this goal. The aim of the study was to assess the effectiveness of SAPB on postoperative VATS analgesia.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date December 1, 2016
Est. primary completion date December 1, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients who were in the American Society of Anesthesiologists (ASA) I-III class and underwent video-assisted thoracoscopic surgery (VATS).

Exclusion Criteria:

- Previous history of opioid use preoperatively,

- Allergy to local anesthetics,

- The presence of any systemic infection,

- Uncontrolled arterial hypertension,

- Uncontrolled diabetes mellitus.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Serratus Anterior Plane Block

Drug:
IV patient-controlled analgesia (PCA) tramadol


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Bursa Yüksek Ihtisas Education and Research Hospital

Outcome

Type Measure Description Time frame Safety issue
Other side effect profile side effect profile 24 hours
Other additional analgesic use additional analgesic use 24 hours
Primary Visual Analogue Scale Visual Analogue Scale was used for pain Postoperative 24 hours
Secondary tramadol consumption tramadol consumption Postoperative 24 hour
Secondary Ramsay sedation scale (RSS) Ramsay sedation scale (RSS) 24 hours
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