Pectus Excavatum

10

Review clinical trials related to Pectus Excavatum. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

SPSIPB Versus SAPB for Postoperative Analgesia After Minimally Invasive Repair of Pectus Excavatum

This prospective observational cohort study will compare postoperative analgesic outcomes in patients undergoing minimally invasive repair of pectus excavatum. Participants will be grouped according to the regional analgesia technique applied as part of routine clinical care: serratus posterior superior intercostal plane block or serratus anterior plane block. The primary outcome will be total opioid consumption during the first 24 hours after surgery. Secondary outcomes will include postoperative pain scores, rescue analgesic requirement, opioid-related adverse effects, patient satisfaction, mobilization time, and length of hospital stay.

Participants needed: 80
Trial details
Age: 15-25Biological sex: AllType: ObservationalSponsor: Marmara UniversityUpdated: Jul 13, 2026Locations: 1Duration: 7 Days
Eligibility criteria

Patients aged 15 to 25 years [+4]

Refusal to participate in the study [+9]

Status: Recruiting

Phrenic Infiltration as Cryoanalgesia Adjuvant for Early Postoperative Pain Following the Nuss Procedure

The goal of this observational ambispective study is to compare the effectiveness of two pain management strategies in pediatric patients undergoing the Nuss procedure for pectus excavatum. The main questions it aims to answer are: Does the addition of phrenic Infiltration as Cryo Adjuvant (PhICA) to earlier percutaneous intercostal cryoanalgesia (EPIC) reduce postoperative pain scores compared to EPIC alone? Does the combined EPIC + PhICA technique reduce the need for rescue tramadol compared to EPIC alone? Do the two approaches differ in: length of hospital stay, time to transition to oral therapy, and time to mobilization? Are there any side effects Researchers will compare patients who received EPIC alone to patients who received EPIC + PhICA to see if the combined technique provides superior pain control. Participants: Received either EPIC alone or EPIC combined with PhICA as part of their surgical anesthesia plan Had pain levels assessed using the Numeric Rating Scale (NRS) at regular postoperative intervals Were monitored for rescue tramadol requirements, medicaments taken, length of hospital stay, and mobilization timing Were monitored for any technique-related complication

Participants needed: 50
Trial details
Age: 14+Biological sex: AllType: ObservationalSponsor: Papa Giovanni XXIII HospitalUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

patients who undergo minimally invasive repair at the pediatric surgery departme...

patients who refuse OR whose parents refuse to participate in the study

Status: Recruiting

The BRIDGE Pain Study

The purpose of the study is to discover at least two distinct Musculoskeletal pain subtypes. These types are caused by different brain-and-immune system signals that affect how the body feels pain, and they are also shaped by a person's biology, psychology, and social environment. Aim 1. We want to sort adolescents and young adults with long lasting muscle and bone pain into two different groups. To do this, we will look at participants' childhood medical histories, past treatments, when their pain started, the sex they were assigned at birth, what their pain feels like now, tests of how their body senses pain, and immune system markers found in their blood. We think we will find at least two different types of chronic pain groups, plus one group of patients who had a higher risk for pain (because of a rheumatic disease or past surgery) but never developed long term pain. Aim 2. We want to find out if certain patterns of inflammation in the body change how nerve cells react to pain. Aim 3: We want to understand how different biological, psychological, and social factors are connected to the chronic pain groups we identified. We think we will find certain mental, behavioral, and social risks-as well as protective factors-that help explain why some people develop long-lasting pain and others do not. We expect these factors to play different roles in each pain group, including the group that does not develop chronic pain.

Participants needed: 600
Trial details
Age: 14-26Biological sex: AllType: ObservationalSponsor: Children's Hospital Medical Center, CincinnatiUpdated: May 22, 2026Locations: 1Duration: 4 Weeks
Eligibility criteria

Diagnosis of rheumatic/autoimmune disease/pain condition or surgery prior to age...

They have active disease, or Other major medical comorbidities have developed af...

Status: Recruiting

Field-test and Psychometric Validation of the Pectus Excavatum Evaluation Questionnaire in the Dutch Pectus Excavatum Population

A questionnaire that can measure disease severity from the patients perspective in patients with pectus excavatum already exists in English (Pectus Excavatum Evaluation Questionnaire; PEEQ). This questionnaire was recently translated into Dutch. Before this Dutch version can be used, it needs to be tested by a number of patients. Data will be collected at three moments: 1. Preoperatively: The PEEQ will be completed on paper during the outpatient clinic visit. 2. Postoperatively: The PEEQ will be completed electronically 2 months post-surgery. 3. Test-retest reliability: The PEEQ will be administered electronically at least two weeks after a previous assessment.

Participants needed: 66
Trial details
Age: 12-18Biological sex: AllType: ObservationalSponsor: Erik de LoosUpdated: Mar 25, 2026Locations: 1
Eligibility criteria

Eligible participants will be pectus excavatum patients aged 12 to 18 years old...

Exclusion criteria will be the inability of the patient or their parent/guardian...

Status: Recruiting

Intraoperative Cryoanalgesia Versus Thoracic Epidural Block in MIRPE (Minimally Invasive Repair of Pectus Excavatum)

The main objective of this study is to compare epidural blockade with cryoanalgesia of the intercostal nerves as an analgesic method in the postoperative period of minimally invasive repair of pectus excavatum (MIRPE).

Participants needed: 40
Trial details
Age: 13+Biological sex: AllType: InterventionalSponsor: University of Sao PauloUpdated: Feb 24, 2026Locations: 1
Eligibility criteria

Having pectus excavatum; [+1]

Age < 13 years at the time of the procedure; [+8]

Status: Recruiting

Comparative Analysis Of Modified Vs. Classical Nuss Technique In The Surgical Correction Of Pectus Excavatum "

Although the NUSS technique has become the standard minimally invasive procedure for correcting this deformity, there is a lack of comparative data between the classic and modified NUSS techniques. This research aims to fill this gap by comparing these two methods in terms of various outcomes, such as operative time, postoperative pain control, length of stay in the intensive care unit, and overall cosmetic results. This study addresses the need to optimize surgical techniques to improve patient outcomes. By evaluating these two approaches, the research seeks to provide insights that could lead to better management strategies for patients with pectus excavatum, potentially influencing future clinical practices.

Participants needed: 80
Trial details
Age: 11-18Biological sex: AllType: ObservationalSponsor: University Hospital, Strasbourg, FranceUpdated: Dec 31, 2025Locations: 1
Eligibility criteria

Patients aged 11 to 18 years. [+1]

Patients with a Haller score below 2.25. [+2]

Status: Recruiting

ES Catheter vs Cryoablation After Pectus Surgery

Participants will be randomized to receive ES catheter or cryoablation for pain management after the Nuss procedure. The goal of this study is to compare the following between the two groups: * Time to achieve short-term physical therapy goals and long-term functional outcomes * Compare immediate and long-term postoperative opioid use * Compare numbness on chest of postoperative day 1 and the return of sensation to baseline * Compare the incidence of neuropathic pain and other complications Participants will receive surveys for up to 12 months postoperatively.

Participants needed: 176
Trial details
Age: 12-21Biological sex: AllType: InterventionalSponsor: Children's Hospital Medical Center, CincinnatiUpdated: Sep 18, 2025Locations: 1
Eligibility criteria

Age 12 - 21 years [+2]

Prior pectus repair [+10]

Status: Recruiting

Percutaneous Intercostal Cryoneuromodulation Onset Timing.

Percutaneous Intercostal Cryoneurolysis is a promising technique that addresses acute postoperative pain after Nuss procedure for pectus excavatum. However its onset timing has not yet been determined. A physical examination would assess the variation of chest skin sensitivity to soft touch, cold (water at 4°C), and heat (water at 40°C) through days following the cryoneurolysis procedure.

Participants needed: 20
Trial details
Age: 12-40Biological sex: AllType: ObservationalSponsor: Papa Giovanni XXIII HospitalUpdated: Jul 23, 2025Locations: 1
Eligibility criteria

Patients who are undergoing preoperative percutaneous intercostal cryoneurolysis...

failure to obtain consent

Status: Recruiting

Effectiveness of One-Minute Versus Two-Minute Cryoanalgesia in Nuss Surgery

Intercostal nerve cryoanalgesia has become a popular method for managing postoperative pain after Nuss procedure, showing greater effectiveness compared to epidural anesthesia and patient-controlled analgesia. However, the optimal duration of cryoanalgesia remains unknown. Most protocols use a two-minute cryoablation, although histological studies show similar changes with both one-minute and two-minute applications. This is a pilot, single-center, randomized, double-blind study comparing the effectiveness of one-minute versus two-minute cryoanalgesia in treating pain in patients undergoing correction of pectus excavatum using the Nuss procedure. The aim of the project is to evaluate the validity of the research procedure and determine the sample size for the main study. Preliminary data on postoperative pain intensity, opioid consumption, duration of surgery, length of hospital stay, and complications will be analyzed.

Participants needed: 40
Trial details
Age: 12-18Biological sex: AllType: InterventionalSponsor: Children's Memorial Health Institute, PolandUpdated: May 1, 2025Locations: 1
Eligibility criteria

Pectus excavatum repair with MIRPE [+3]

History of previous thoracic surgeries [+3]

Status: Not yet recruiting

Investigation of the Effectiveness of Telerehabilitation Training in Pectus Excavatum Deformity

The aim of this study is to investigate the effectiveness of telerehabilitation-based exercise training in addition to Vacuum Bell therapy on physical fitness, respiratory functions, posture and psychosocial factors in boys aged between 10-14 years diagnosed with pectus excavatum.

Participants needed: 62
Trial details
Age: 10-14Biological sex: MaleType: InterventionalSponsor: Eastern Mediterranean UniversityUpdated: Oct 10, 2024Locations: 1
Eligibility criteria

Children aged 10-14 [+2]

Those with complex type pectus deformity [+8]