TERMINATED

Pudendal vs Caudal Block for Pediatric Penile Surgery

Conditions

Postoperative Pain Nerve Block Caudal Block Pudendal Block Circumcision Hypospadias Postoperative Analgesia Opioid Consumption Pain Score

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The study will compare recovery profile in children receiving pudendal blocks vs caudal analgesia for ambulatory circumcision or hypospadias repair in children between 6 months and 2 years. The subjects of the study will be randomized to receive either a caudal or a pudendal block.

Official Title

Pudendal vs Caudal Block for Pediatric Penile Surgery

Quick Facts

Study Start:2021-05-01

Study Completion:2024-10-02

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:TERMINATED

Study ID

NCT04840654

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:6 Months to 3 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:CHILD

Inclusion Criteria	Exclusion Criteria
* - Children Aged 6 months -3 years * Scheduled for elective outpatient circumcision or hypospadias repair	* ASA classification ≥ 3 * emergency surgery * history of a complex regional pain syndrome * sacral dimple * known vertebral spinal abnormalities, spinal dysraphism * history of long-term analgesic use * use of any analgesic (e.g., an opioid medication, acetaminophen, or a nonsteroidal anti-inflammatory agent) within 24 hours before surgery * history of renal insufficiency or a bleeding disorder * concurrent additional surgery at another anatomic site * being a ward of the state * a non-English speaking patient or primary caregiver * inability of the primary caregiver to comply with home instructions

Inclusion Criteria

Exclusion Criteria

* - Children Aged 6 months -3 years
* Scheduled for elective outpatient circumcision or hypospadias repair

* ASA classification ≥ 3
* emergency surgery
* history of a complex regional pain syndrome
* sacral dimple
* known vertebral spinal abnormalities, spinal dysraphism
* history of long-term analgesic use
* use of any analgesic (e.g., an opioid medication, acetaminophen, or a nonsteroidal anti-inflammatory agent) within 24 hours before surgery
* history of renal insufficiency or a bleeding disorder
* concurrent additional surgery at another anatomic site
* being a ward of the state
* a non-English speaking patient or primary caregiver
* inability of the primary caregiver to comply with home instructions

Contacts and Locations

Principal Investigator

Leili Khorassani, MD

PRINCIPAL_INVESTIGATOR

University of Chicago

Study Locations (Sites)

University of Chicago Medical Center

Chicago, Illinois, 60637

United States

Collaborators and Investigators

Sponsor: University of Chicago

Leili Khorassani, MD, PRINCIPAL_INVESTIGATOR, University of Chicago

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-05-01

Study Completion Date2024-10-02

Study Record Updates

Study Start Date2021-05-01

Study Completion Date2024-10-02

Terms related to this study

Keywords Provided by Researchers

Nerve Block
Caudal Block
Pudendal Block
Circumcision
Hypospadias
Postoperative Analgesia
Opioid Consumption
Pain Score

Additional Relevant MeSH Terms

Postoperative Pain