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Cryoanalgesia to Prevent Acute and Chronic Pain Following Nuss Procedure

Primary Purpose

Funnel Chest, Excavatum, Pectus

Status
Completed
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
intercostal nerves cryoanalgesia
Sponsored by
Pomeranian Medical University Szczecin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Funnel Chest focused on measuring nuss procedure, ERAS, cryolesia, cryoanalgesia

Eligibility Criteria

10 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients undergoing pectus excavatum repair with modyfied minimal invasive thoracoscopic NUSS technique
  • aged 10 years or above 10
  • informed consent signed for cryoanalgesia

Exclusion Criteria:

  • Age of 9 years or below
  • Refuse to receive cryoanalgesia or regional analgesia as primary pain relief
  • Any contraindication to cryoanalgesia
  • Difficult follow-up for geographical reasons and/or impossibility by the patient to understand how to perform self-measurements

Sites / Locations

  • Pomeranian Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

"the before" group

"the after" group

Arm Description

Control group as a standard therapy in Poland (regional analgesia: intrapleural or bilateral erector spine plane block added to multimodal analgesia).

During modyfied Nuss thoracoscopy the intraoperative Cryolesia of at least 5 intercostal nerves added to regional analgesia: bilateral erector spine plane block and multimodal therapy.

Outcomes

Primary Outcome Measures

The worse pain occurence during first 24 hours after operation
Numeric pain score. Range from 0 to 10.

Secondary Outcome Measures

Analgesic consumption post operation
Total analgesic (including opioids) consumption for previous 24 hours
Thoracic hypo-aesthesia occurence
Cold test assessment (Yes/No)
Assessment of sleeping quality
Collect difficulties of sleeping due to pain? (binary answer: yes or no; not based on a scale or instrument)
Postoperative nausea and vomiting (PONV) occurence
binary answer: yes or no; not based on a scale or instrument
Residual wound or chest pain occurence
The chest or wound chronic pain occurrences
Total narcotic use post-operation
Total dose and number of days of opioids used during hospitalization
Cost Analysis
total costs of hospitalization
Duration of hospitalization
the length of the time (in days) spent in the hospital

Full Information

First Posted
September 29, 2022
Last Updated
March 27, 2023
Sponsor
Pomeranian Medical University Szczecin
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1. Study Identification

Unique Protocol Identification Number
NCT05570097
Brief Title
Cryoanalgesia to Prevent Acute and Chronic Pain Following Nuss Procedure
Official Title
Cryoanalgesia in Combination With the Novel Prehabilitation Program Back on Feet Are the Essential Parts of Enhanced Recovery Protocol in the Minimal Invasive Modyfied Nuss Procedure of Children With Funnel Chest Deformation.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
September 28, 2022 (Actual)
Primary Completion Date
October 10, 2022 (Actual)
Study Completion Date
December 10, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Pomeranian Medical University Szczecin

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This Study study compared standard therapy (multimodal and regional analgesia) versus a novel approach (Cryoanalgesia combined with bilateral erector spine plane block and multimodal analgesia) in subjects undergoing minimal invasive modyfied Nuss procedure (thoracoscopy).
Detailed Description
Funnel chest deformation is a great challenge for therapeutic teams due to severe pain in the postoperative period as well as chronic pain. The use of many analgesic drugs, including opioids, is associated with adverse side effects, difficulties with rehabilitation, an increased risk of complications, prolonged hospitalisation, and the cost of the procedure. Cryoanalgesia as a part of multimodal analgesia along with the education and prehabilitation of the patient according to the novel original educational - training application 'Back on Feet' as well as the interdisciplinary care in accordance with the enhanced recovery after surgery (ERAS) protocol, which has a real impact on the optimisation of perioperative care. This Before - After Study is a single institution pilot study designed to compare standard therapy (control group: regional analgesia: intrapleural or bilateral erector spine plane block) versus a novel approach (interventional group: Cryoanalgesia combined with bilateral single shot erector spine plane block) to address the need for better management of acute and long-term pain in the pediatric population diagnosed with funnel-chest and treated using the modyfied Nuss method. First group received a standard care according to Polish guidelines. The data of control group analysed and the interdisciplinary team work protocol will be introduced to the interventional group. The interventional group was prepared according to prehabilitation with the 'Back on feet' application and perioperative ERAS protocols. The patients of interventional group received intraoperative cryoanalgesia using the Cryo-S Painless device (Metrum - Cryoflex Polska Limited) as an additional procedure to multimodal analgesia. This is the first time that the cryoanalgesia procedure was performed in children in Poland. The aims of the study were the assessment the effectiveness of cryoanalgesia as a method of acute and long-term pain control, safety of the method and the impact of preoperative preparation according to the 'Back on Feet' program introduced as a part of ERAS protocol. Specific Aim 1: To determine if, compared with current analgesia, the addition of cryoanalgesia decreases the incidence and severity of post-surgical pain. Hypothesis 1a (primary): The severity of surgically-related pain was significantly decreased from postoperative day 2 with the addition of cryoanalgesia as compared with patients receiving solely standard-of-care treatment. Hypothesis 1b: The incidence and severity of chronic pain was significantly decreased 3 months following surgery with the addition of cryoanalgesia as compared with patients receiving solely standard-of-care treatment. Specific Aim 2: To determine if, compared with current analgesia, the addition of cryoanalgesia improves postoperative functioning. Hypothesis 2a: Following modyfied Nuss procedure the range of motion and independence was significantly increased in the 2 postoperative day following operation with the addition of cryoanalgesia as compared with patients receiving solely standard-of-care treatment. The results were compared in terms of demographics, pain levels, side effects of the pain relief medications in the postoperative period, quality and length of rehabilitation, patient satisfaction using the Quality of Life by modyfied Nuss questionnaire, and the total costs of hospitalization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Funnel Chest, Excavatum, Pectus
Keywords
nuss procedure, ERAS, cryolesia, cryoanalgesia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
Before - after study: First: control group as a standard treatment in Poland, review, then: interventional group
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
"the before" group
Arm Type
No Intervention
Arm Description
Control group as a standard therapy in Poland (regional analgesia: intrapleural or bilateral erector spine plane block added to multimodal analgesia).
Arm Title
"the after" group
Arm Type
Experimental
Arm Description
During modyfied Nuss thoracoscopy the intraoperative Cryolesia of at least 5 intercostal nerves added to regional analgesia: bilateral erector spine plane block and multimodal therapy.
Intervention Type
Device
Intervention Name(s)
intercostal nerves cryoanalgesia
Intervention Description
Intraoperative Cryolesia of at least 5 intercostal nerves added to regional analgesia: bilateral erector spine plane block and multimodal therapy.
Primary Outcome Measure Information:
Title
The worse pain occurence during first 24 hours after operation
Description
Numeric pain score. Range from 0 to 10.
Time Frame
up to 24 hours after operation
Secondary Outcome Measure Information:
Title
Analgesic consumption post operation
Description
Total analgesic (including opioids) consumption for previous 24 hours
Time Frame
Postoperative days 0, 1, 2, 3, 4, 5,6, as well as months 1 and 3
Title
Thoracic hypo-aesthesia occurence
Description
Cold test assessment (Yes/No)
Time Frame
up to 24 hours after operation
Title
Assessment of sleeping quality
Description
Collect difficulties of sleeping due to pain? (binary answer: yes or no; not based on a scale or instrument)
Time Frame
Postoperative days 1, 2, 3, 4, 5 ,6
Title
Postoperative nausea and vomiting (PONV) occurence
Description
binary answer: yes or no; not based on a scale or instrument
Time Frame
Postoperative days 1, 2, 3, 4, 5 ,6
Title
Residual wound or chest pain occurence
Description
The chest or wound chronic pain occurrences
Time Frame
Postoperative months 1, 3
Title
Total narcotic use post-operation
Description
Total dose and number of days of opioids used during hospitalization
Time Frame
0-6 postoperative days
Title
Cost Analysis
Description
total costs of hospitalization
Time Frame
estimated 1 week
Title
Duration of hospitalization
Description
the length of the time (in days) spent in the hospital
Time Frame
estimated 1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients undergoing pectus excavatum repair with modyfied minimal invasive thoracoscopic NUSS technique aged 10 years or above 10 informed consent signed for cryoanalgesia Exclusion Criteria: Age of 9 years or below Refuse to receive cryoanalgesia or regional analgesia as primary pain relief Any contraindication to cryoanalgesia Difficult follow-up for geographical reasons and/or impossibility by the patient to understand how to perform self-measurements
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jowita Biernawska, MD PhD
Organizational Affiliation
Pomeranian Medical Universitet Szczecin
Official's Role
Study Director
Facility Information:
Facility Name
Pomeranian Medical University
City
Szczecin
ZIP/Postal Code
71-252
Country
Poland

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
We invite others researchers to collaboration as multicenter study.
IPD Sharing Time Frame
up to 12 months from the beginning of the study
IPD Sharing Access Criteria
by contact to Principal Investigator
Citations:
PubMed Identifier
30935731
Citation
Graves CE, Moyer J, Zobel MJ, Mora R, Smith D, O'Day M, Padilla BE. Intraoperative intercostal nerve cryoablation During the Nuss procedure reduces length of stay and opioid requirement: A randomized clinical trial. J Pediatr Surg. 2019 Nov;54(11):2250-2256. doi: 10.1016/j.jpedsurg.2019.02.057. Epub 2019 Mar 17.
Results Reference
result

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Cryoanalgesia to Prevent Acute and Chronic Pain Following Nuss Procedure

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