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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00512044
Other study ID # P07/CHV
Secondary ID
Status Withdrawn
Phase Phase 4
First received
Last updated
Start date October 2007
Est. completion date May 2008

Study information

Verified date February 2020
Source University of Lausanne Hospitals
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether local or general anaesthesia in stapled hemorrhoidectomy leads to a shorter operation time with a better patient comfort.


Description:

Hemorrhoids are a frequent disease with the need of surgical intervention in 10-20% of the patients. The stapled hemorrhoidectomy according to Longo under general anesthesia (or spinal) is considered standard of care [1]. Cohort studies show that a pudendal bloc with local anesthesia is safe and efficient [2-4]. The majority of procedures are actually performed in private clinics or in an ambulatory setting underlining the importance of economic issues such as procedure time (anesthesia and operation time) and hospital stay.

We hypothesize that stapled hemorrhoidectomy under local anaesthesia shortens anaesthesia time and hospital stay and reduces costs with no disadvantages regarding pain, satisfaction and complication rate.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date May 2008
Est. primary completion date November 2007
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- Hemorrhoids grade III suitable for elective stapled hemorrhoidectomy

Exclusion Criteria:

- Age < 18 years

- No informed consent

- Emergency situation

- Contraindication to either anaesthesia method

- Patients not speaking french or german.

- Additional anal pathology (fissure, tumour).

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Local anesthesia (pudendal block)
local anesthesia as indicated
general anesthesia (spinal and general)
general according to guidelines

Locations

Country Name City State
Switzerland Department of Visceral Surgery, University Hospital Center Lausanne

Sponsors (1)

Lead Sponsor Collaborator
University of Lausanne Hospitals

Country where clinical trial is conducted

Switzerland, 

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