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NCT01003561 Clinical Trial

Hemodynamic Changes of Upper and Lower Extremities After Spinal Anesthesia

Hypertension Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT01003561
Other study ID # 2009-TURP
Secondary ID
Status Not yet recruiting
Phase N/A
First received October 27, 2009
Last updated October 27, 2009

Study information
Verified date October 2009
Source Yonsei University
Contact Jeong-Yeon Hong, MD
Email jenyhongg@yuhs.ac
Is FDA regulated No
Health authority South Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the changes of venous flow, volume, and resistance in upper (basilic v.) and lower (popliteal v.) extremities of the elderly healthy patients compared with elderly hypertensive patients who undergoing spinal anesthesia for transurethral prostatectomy.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 40
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Male
Age group 65 Years and older
Eligibility Inclusion Criteria:

- > 65yr men

- who undergoes spinal anesthesia for elective TURP

- normotensive/hypertensive

Exclusion Criteria:

- vascular disease

- contraindications for spinal anesthesia

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator)

Related Conditions & MeSH terms

Intervention

Procedure:
• spinal anesthesia for surgery
spinal anesthesia (T10) for elective TURP surgery

Locations
Country Name City State
Korea, Republic of Severance Hospital, Yonsei University Seoul

Sponsors (1)
Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Blood flow during 30 min after spinal anesthesia No
Primary Blood volume during 30 min after spinal anesthesia No
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