ReSECT: Registry of the Spanish Society of Thoracic Surgery

Sponsor
Sociedad Española de Cirugía Torácica (Other)
Overall Status
Recruiting
CT.gov ID
NCT05600569
Collaborator
(none)
30,000
1
120
250

Study Details

Study Description

Brief Summary

ReSECT is a project promoted by the Spanish Society of Thoracic Surgery with the aim not only to become an indefinite, dynamic and inclusive registry, but also to establish a common structural framework for the development of future multicentre projects in the field of thoracic surgery in Spain.

The goal of this nationwide prospective observational registry is:
  • To develop and validate forecasting tools based on powerful computational methods with the goal of assisting in decision-making and improving quality of care.

  • To evaluate the progressive implementation of certain surgical techniques that are on the rise, new technologies and future health programs.

  • To be aware of our results as specialty and professionals and to serve as a permanent benchmarking instrument in thoracic surgery.

The first part of ReSECT, based on a personal registry design, will contemplate any thoracic surgical procedure performed by thoracic surgeons and residents in thoracic surgery in our country. Additionally, the Spanish thoracic surgery departments that voluntarily accept to collectively participate will contribute to specific surgical processes focused on certain procedures with specific objectives to be progressively implemented.

The first and only surgical process implemented since the start of the ReSECT project will focus on patients to undergo anatomical lung resection with special interest in those cases whose reason for intervention was lung cancer.

The main questions to answer in case of that first surgical process include:
  • What is the performance of current predictive models for perioperative and oncological outcomes in our country?

  • How could we modify previous predictive models to improve their performance?

  • What is the implementation of current guideline recommendations in our country and across institutions?

  • What is the potential impact of deviations from current recommendations?

  • What is my performance compared to the rest of the thoracic surgical departments in my country in terms of perioperative and oncological outcomes?

ReSECT does not consider prespecified comparison groups of patients.

Detailed Description

ReSECT is intended for SECT members including thoracic surgery specialists and residents with professional practice in Spain, as well as thoracic surgery departments in our country.

Participation in ReSECT may be at the individual level (personal surgical registry) or by department (ReSECT surgical processes). Those thoracic surgery departments interested in participating in a surgical process implemented in ReSECT must be represented by a single responsible hospital user.

ReSECT will be a clinical registry based on surgical procedures. The retrospective and prospective nature of the personal surgical record will be determined by the user's ability to include records of patients who underwent surgery prior to the approval of the current project. However, the "retrospective patients" to be included must belong to the centre associated with each user at the time of registering on the platform. In other words, it will not be feasible to include patients operated on in other institutions where the professional had previously worked.

The first ReSECT surgical process about anatomical lung resections and the successive processes that are to be created in the future, will only contemplate patients operated on prospectively with respect to the date of approval of each surgical process.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
30000 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Registry of the Spanish Society of Thoracic Surgery (ReSECT)
Actual Study Start Date :
Jan 1, 2023
Anticipated Primary Completion Date :
Dec 31, 2032
Anticipated Study Completion Date :
Dec 31, 2032

Arms and Interventions

Arm Intervention/Treatment
All the target population

Patients who will undergo any surgical procedure in a Spanish Thoracic Surgery Department

Outcome Measures

Primary Outcome Measures

  1. Rate of perioperative mortality [From surgery date to hospital discharge day or within ninety days.]

    Mortality during hospitalization or that occurred within thirty and ninety days after surgery.

  2. Rate and severity of perioperative morbidity [From surgery date to hospital discharge day or within thirty days.]

    Complications occurred during hospitalization will be classified into 3 groups: cardiovascular, respiratory and other type of complications. Each of these groups of complications will be classified based on the most severe specific complication according to the Clavien-Dindo classification (grade I, II, IIIa, IIIb, IVa, IVb, V). Specific respiratory complications: initial ventilator support > 48h, re-intubation, ARDS, pneumonia, atelectasis, air leak > 5 days, pulmonary embolism, acute respiratory failure, phrenic palsy, pulmonary infarction, pneumothorax, pleural effusion, subcutaneous emphysema, chylothorax, bronchopleural fistula, others. Specific cardiovascular complications: blood transfusion, arrhythmia, myocardial infarction, heart failure, cerebrovascular accident, deep vein thrombosis, others. Other type of complications: no-respiratory sepsis, wound infection, renal failure, delirium, others.

  3. Overall survival [Five-year follow-up after surgery]

    Overall survival after anatomical resection for lung cancer. The outcome will include exitus for any reason.

  4. Disease specific survival [Five-year follow-up after surgery]

    Disease free survival after anatomical resection for lung cancer. The outcome will include exitus for lung cancer progesssion.

  5. Recurrence free survival [Five-year follow-up after surgery.]

    Recurrence free survival after anatomical resection for lung cancer. The outcome will include recurrence of lung cancer.

Secondary Outcome Measures

  1. Rate of hospital readmission [From hospital discharge day to thirty days afterwards.]

    Readmissions within thirty days of discharge from hospital for reasons related to the surgical procedure.

  2. Diagnosis and severity of complications during hospital readmission. [From hospital readmission date to hospital discharge day or within 30 days]

    Primary reason for readmission and severity of complications from readmission date to hospital discharge day

  3. Unplanned Intensive Care [From day of surgery to day of hospital discharge or within 30 days]

    Rate of patients who required unplanned intensive care unit admission

  4. Rate of patients that required surgical reintervention [From surgery date to hospital discharge day and from hospital readmission date to hospital discharge day or within 30 days]

    Surgical reinterventions will be considered when related to complications secondary to the main surgical procedure. This rate will be calculated: number of patients that required reintervention during main hospitalization of after readmission / total number of patients.

  5. Rate of patients with functional status classified as independent, partially independent of totally dependent [The day of hospital discharge or within 30 days after surgery.]

    Functional status will be referred to patient ability to perform basic and instrumental activities of daily living. Patients will be classified into: Independent: autonomous patient to carry out most of the instrumental activities of daily living (pet care, raising kids, use of communication systems, mobility in the community, management of financial issues, health care and support, maintain a home, food preparation and cleaning, security procedures and emergency responses, go shopping). Partially dependent: autonomous patient for most of the basic activities of daily living (bath / shower, locker room, feeding, sphincters control, functional mobility, care of personal technical aids, personal hygiene and grooming, sexual activity, go sleeping, toilet hygiene), but unable to perform most instrumental activities of daily living. Totally dependent: patient who requires help to carry out most of the basic activities of daily living.

  6. Rate of patients with invasive mediastinal staging [From three months before surgery to surgical intervention date]

    Number of patients with diagnosis of lung cancer who underwent invasive staging of the mediastinum / number of patients with lung cancer who meet criteria for invasive staging of the mediastinum according to current guidelines.

  7. Rate of complete resection for lung cancer [During the surgery]

    Number of patients with lung cancer who underwent complete resection / number of patients with lung cancer who underwent surgical resection.

  8. Distribution of patients according to type of lymphadenectomy [During the surgery]

    Patients operated on for lung cancer will be classified according to type of lymphadenectomy performed into: Minor Lymphadenectomy. Lobe-specific systematic lymph node dissection: exeresis of the mediastinal tissue that contains the lymph nodes of certain lymph node stations is performed, depending on the location of the tumor. Tumor in the right upper lobe or middle lobe: 2R, 4R and 7. Tumor in the lower right lobe: 4R, 7, 8 and 9. Tumor in the upper left lobe: 5, 6 and 7. Tumor in the lower left lobe: 7, 8 and 9. Systematic lymph node dissection: dissection and exeresis of the mediastinal tissue that contains the lymph nodes following the anatomical limits. It is recommended that at least 3 mediastinal lymph node stations be excised, always including the subcarinal, in addition to the hilar and intrapulmonary stations.

  9. Rate of occult pN2 disease [During the surgery]

    Number of patients operated on for lung cancer with pathological N2 disease and clinical N0-N1 disease / Number of patients operated on for lung cancer with clinical N0-N1 disease.

  10. Mean postoperative stay [From day of surgery to day of hospital discharge or within 3 months.]

    Number of days of hospitalization after surgery

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

The inclusion criteria will depend on the section of the registry to be considered.

  • Personal registry: patients undergoing any type of surgical intervention.

  • Registry of surgical processes by departments: patients undergoing an anatomical pulmonary resection as the first process to be implemented at the time ReSECT is to be established.

Exclusion Criteria:
  • Patients who could reject to participate in this study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital Universitario Miguel Servet Zaragoza Spain 50009

Sponsors and Collaborators

  • Sociedad Española de Cirugía Torácica

Investigators

  • Study Director: Raúl Embún, PhD, Hospital Universitario Miguel Servet / raulembun@gmail.com / Phone: +34 635 492179

Study Documents (Full-Text)

More Information

Additional Information:

Publications

Responsible Party:
Sociedad Española de Cirugía Torácica
ClinicalTrials.gov Identifier:
NCT05600569
Other Study ID Numbers:
  • sect/resect/01
First Posted:
Oct 31, 2022
Last Update Posted:
Jan 4, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sociedad Española de Cirugía Torácica
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 4, 2023