Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05184647
Other study ID # RECHMPL21_0712
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date January 16, 2022
Est. completion date December 30, 2022

Study information

Verified date December 2021
Source University Hospital, Montpellier
Contact Nicolas KALFA, MD
Phone 00334 67 33 87 84
Email n-kalfa@chu-montpellier.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Partial splenectomy or total splenectomy are the two surgical treatment of non-malignant hemoglobinoptahie. The aim of this treatment is to decrease transfusion. The main risk is infectious in total splenectomy, that's why partial splenectomy was suggest. But the efficiency of partial splenectomy decrease over time and a totalisation could be mandatory.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date December 30, 2022
Est. primary completion date June 30, 2022
Accepts healthy volunteers No
Gender All
Age group N/A to 18 Years
Eligibility Inclusion criteria: - Children between 0- 18 years olds - Total or partial splenectomy - Non malignant hémoglobinopathies Exclusion criteria: - Total or partial splenectomy outside of non malignant hemoglobinopathies

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France University hospital of Montpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Compared the effectiveness with the number of transfusion Compared the effectiveness with the number of transfusion after the surgery between total and partial Febrile urinary tract infection was defined as a positive urine examination with a single bacteria with more than 10.5 cfu/mL and more than 10.4 leukocytes/ml associated with fever above 38.5°C and C-reactive protein (CRP) above 50 mg/ Day 1
Secondary Number of infectious event in total and partial splenectomy Number of infectious event in total and partial splenectomy Day 1
Secondary number of totalisation in partial number of totalisation in partial Day 1
See also
  Status Clinical Trial Phase
Completed NCT03117192 - Zinc Supplementation on Cellular Immunity in Thalassemia Major Phase 4
Not yet recruiting NCT06025487 - Meningococcal B Vaccine in Patients With Asplenia Phase 2
Completed NCT04645550 - Apixaban, Warfarin and Aspirin Prevents Portal Vein Thrombosis in Patients After Laparoscopic Splenectomy(ESAWAAPT) Phase 4
Recruiting NCT05325424 - The Effect of Laparoscopic Splenectomy on Liver Reserve Function for Cirrhosis Patients N/A
Recruiting NCT05338294 - The Effect of Laparoscopic Splenectomy and Azygoportal Disconnection on the Immune Function for Cirrhosis Patients N/A
Recruiting NCT05339269 - The Effect of Laparoscopic Splenectomy on the Immune Function for Cirrhosis Patients N/A
Recruiting NCT05325437 - The Effect of Laparoscopic Splenectomy and Azygoportal Disconnection on Liver Reserve Function for Cirrhosis Patients N/A
Completed NCT03571399 - A Nationwide Italian Survey on Asplenia
Completed NCT04056507 - Immunological Markers in Adult Patients With Immune Thrombocytopenic Purpura