CClinicalTrials.gg
CompletedNCT02401087Updated Aug 28, 2019

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

An observational study in Varicocele, sponsored by Ospedale di Circolo - Fondazione Macchi. Completed at 1 site in Italy. Open to male participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-08-28.

Sponsored by Ospedale di Circolo - Fondazione Macchi · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
40
Ages
18 Years and older
Sex
Male
01

Study 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.

02

Conditions studied

  • Varicocele

Browse trials for

03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Male
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

The patients will be identified as potentially were to be enrolled in the preoperative anesthetic visit.

Inclusion criteria

  • Male
  • ASA I-II
  • No mental alteration

Exclusion criteria

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
04

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
40 participants (actual)
Patient registry
No

Interventions

  • ProcedureAnaesthesiological procedure
05

What researchers measure

Primary outcomes

  1. discharge time

    check the elapsed time between the induction of anesthesia and obtaining discharge criteria, urination and deambulation, from the Department of Day Surgery.

    Time frame: one day

Secondary outcomes

  1. Difference in the onset of acute post-operative pain

    Time frame: four days

  2. Check the occurence of any side effects

    Time frame: three months

  3. Clinical evaluation of patients at 1 and 3 months after surgery (possibility of chronic pain)

    Time frame: three months

06

Study locations

1 site
  • Department of Day Surgery Ospedale di Circolo Varese
    Varese, VA 21100, Italy
07

Registry details

Key details

Study ID
NCT02401087
Lead sponsor
Ospedale di Circolo - Fondazione Macchi
Responsible party
Andrea Luigi Ambrosoli (M.D., Ospedale di Circolo - Fondazione Macchi) — Principal investigator
First posted
Mar 27, 2015
Start date
May 2014
Primary completion
May 2015
Completion
Aug 2016
Last update
Aug 28, 2019

Study contacts

Stefania Turconi, MD
principal investigator · University Hospital Varese

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2019. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion