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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03704441
Other study ID # KangnamAnes
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 1, 2018
Est. completion date September 1, 2020

Study information

Verified date April 2020
Source Hallym University Kangnam Sacred Heart Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

As people age, the incidence of prostate hyperplasia increases. So patients under Transurethral Resection of Prostate(TURP) or Holmium Laser Ennucleation of Prostate(HoLEP) are mostly ole age people. Most old age patient has several underlying disease. So patients can develop high mortality and morbidity. Most surgeries for Prostate Resection are taken under Spinal anesthesia. Adequate block level for Prostate Resection is T10. But sometimes, old age patients can develop severe complication after spinal anesthesia. So we started this study to know the adequate drug concentration for Spinal anesthesia taken for Prostate Resection surgery.


Description:

As people age, the incidence of prostate hyperplasia increases. So patients under Transurethral Resection of Prostate(TURP) or Holmium Laser Ennucleation of Prostate(HoLEP) are mostly ole age people. Most old age patient has several underlying disease. So patients can develop high mortality and morbidity. Most surgeries for Prostate Resection are taken under Spinal anesthesia. Adequate block level for Prostate Resection is T10. But sometimes, old age patients can develop severe hypotension and vital unstability due to unintentional high sensory and motor blocks. These complications are due to the decreased cerebrospinal fluid volume with increase of age. So we started this study to know the adequate drug concentration for Spinal anesthesia taken for Prostate Resection surgery.


Recruitment information / eligibility

Status Completed
Enrollment 13
Est. completion date September 1, 2020
Est. primary completion date May 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 65 Years to 100 Years
Eligibility Inclusion Criteria: - Patients scheduled for TURP & HoLEP under spinal anesthesia - Male between 65 and 100 - The American Society of Anesthesiologists physical status class 1 or 2 Exclusion Criteria: - Patients with coagulopathy - Patients with infectious disease - Patients with a drug allergy - Patients under 50kg or over 100kg - In case of switching to general anesthesia

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Bupivacaine
bupivacaine dose

Locations

Country Name City State
Korea, Republic of Kangnam sacred heart hospital Seoul Yeongdeungpo-gu

Sponsors (1)

Lead Sponsor Collaborator
Hallym University Kangnam Sacred Heart Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary ED50 and ED95 of intrathecal hyperbaric bupivacaine with fentanyl for transurethral prostatectomy in elderly patients ED50(50% Effective dose) and ED95(95% Effective dose) of intrathecal hyperbaric bupivacaine with fentanyl for transurethral prostatectomy in elderly patients 2years
Secondary comparison of incidence of complications(hypotension, nausea/vomiting and shivering) during perioperative period comparison of incidence of complications(hypotension, nausea/vomiting and shivering) during perioperative period 2years
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