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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02401087
Other study ID # Var-001
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 2014
Est. completion date August 2016

Study information

Verified date August 2019
Source Ospedale di Circolo - Fondazione Macchi
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this observational study was to evaluate, based on the intraoperative anesthetic that is routinely carried out at the Department of Day Surgery, the difference in timing of the patient's discharge from the hospital (ie when the patient has autonomous demabulation and urination spontaneous) in patients undergoing correction of varicocele according Marmar.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date August 2016
Est. primary completion date May 2015
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Male

- ASA I-II

- No mental alteration

Exclusion Criteria:

- Chronic pain

- Allergies to local anaesthetics, acetaminophen,oppioids

- ASA III - IV

- Postoperative discharge to ICU

- Epatic or renal failure

- Mental status alteration

- Coagulopathy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Anaesthesiological procedure


Locations

Country Name City State
Italy Department of Day Surgery Ospedale di Circolo Varese Varese VA

Sponsors (1)

Lead Sponsor Collaborator
Ospedale di Circolo - Fondazione Macchi

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary discharge time check the elapsed time between the induction of anesthesia and obtaining discharge criteria, urination and deambulation, from the Department of Day Surgery. one day
Secondary Difference in the onset of acute post-operative pain four days
Secondary Check the occurence of any side effects three months
Secondary Clinical evaluation of patients at 1 and 3 months after surgery (possibility of chronic pain) three months
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