Actively Recruiting

Age: 0Years - 1Year
All Genders
ID06909227

Relevance of Veinous Lactates Dosage at the End of a Surgical Procedure to Predict Postoperative Complications in Children 0-1 Years

Led by Hôpital Armand Trousseau · Updated on 2025-05-01

500

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying whether the amount of veinous lactate measured at the end of surgery is linked to complications within 3 months after surgery in infants aged 0 to 1 year. This observational study focuses on young children undergoing surgery under general anesthesia, excluding those having day-case or cardiac surgery. The goal is to see if higher lactate levels could predict post-operative problems in this age group, similar to findings in adults. The study involves infants under 1 year old who undergo non-cardiac surgery with general anesthesia. Blood samples for lactate measurement are taken routinely before the child wakes up from anesthesia, using the intravenous line placed for anesthesia. The investigation centers on routine surgical procedures without additional experimental treatments. During the study, infants' blood lactate levels are measured at the end of surgery, and researchers monitor for any complications occurring within 3 months after surgery. Data collection includes routine blood sampling from the anesthesia IV line. The main outcome is the occurrence of post-operative complications during the follow-up period. Participation duration covers the surgery day plus 3 months of monitoring for any complications.

CONDITIONS

Brief Title

Relevance of Veinous Lactates to Predict Postoperative Complications in Children 0-1 Years

Who Can Participate

Age: 0Years - 1Year
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Surgery under general anesthesia
  • Age less than 1 year
Not Eligible

You will not qualify if you...

  • Ambulatory (day-case) surgery
  • Cardiac surgery
  • Preoperative hemodynamic instability
  • Weight less than 2 kilograms

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surgery and Immediate Post-operative Care

Duration - Day of surgery

Participants undergo surgery under general anesthesia and immediate post-operative care.

1 visit (in-person)

Post-operative Follow-up

Duration - Up to 3 months after surgery

Participants are monitored for post-operative complications after surgery.

Regular follow-up visits during this period

Trial Site Locations

Total: 1 location

1

Armand Trousseau University Hospital

Paris, France, 75012

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Research Team

M

Mireille Nasr, MD

N

Nada Sabourdin, MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial