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The Anaesthesiological Approach to Varicocele Correction in Outpatients Setting: an Observational Analysis

The Anaesthesiological Approach to Varicocele Correction in Outpatients Setting: an Observational Analysis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02401087
Enrollment
40
Registered
2015-03-27
Start date
2014-05-31
Completion date
2016-08-31
Last updated
2019-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Varicocele

Brief 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.

Interventions

PROCEDUREAnaesthesiological procedure

Sponsors

Ospedale di Circolo - Fondazione Macchi
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
discharge timeone daycheck the elapsed time between the induction of anesthesia and obtaining discharge criteria, urination and deambulation, from the Department of Day Surgery.

Secondary

MeasureTime frame
Difference in the onset of acute post-operative painfour days
Check the occurence of any side effectsthree months
Clinical evaluation of patients at 1 and 3 months after surgery (possibility of chronic pain)three months

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026