A Study to Compare Quality of Life and Satisfaction in Primary Immunodeficient Patients Treated With Subcutaneous Injections of Gammanorm® 165 mg/mL Administered With Two Different Delivery Devices: Injections Using Pump or Rapid Push
A Randomised, Cross-over Study to Compare Quality of Life and Satisfaction in Primary Immunodeficient Patients Treated With Subcutaneous Injections of Gammanorm® 165 mg/mL Administered With Two Different Delivery Devices: Injections Using Pump or Rapid Push
1 other identifier
interventional
30
4 countries
12
Brief Summary
A randomised, cross-over study to compare quality of life and satisfaction in primary immunodeficient patients treated with subcutaneous injections of Gammanorm® 165 mg/mL administered with two different delivery devices: injections using pump or rapid push.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_4
Started Jul 2015
Typical duration for phase_4
12 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 1, 2015
CompletedFirst Posted
Study publicly available on registry
July 20, 2015
CompletedStudy Start
First participant enrolled
July 29, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 11, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
December 11, 2017
CompletedApril 9, 2019
April 1, 2019
2.4 years
July 1, 2015
April 5, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
To compare satisfaction (LQI questionnaire, factor I: treatment interference) in PID patients receiving subcutaneous injections of Gammanorm® 165 mg/mL by delivery device used.
Each patient will be treated for two consecutive periods of three months each according to the sequence assigned based on the cross-over design (syringe and then pump, or pump and then syringe) without any intermediate washout period. The total duration of study treatment will therefore be 6 months for each patient. Assessment will be conducted via the LQI scale.
Participants will be followed for a total of 6 months
Secondary Outcomes (1)
To compare the other quality of life scores
Participants will be followed for a total of 6 months
Study Arms (2)
Chrono Super PID then Generic Syringe - Gammanorm
OTHEREach patient will receive the study treatment using each of the two studied delivery devices according to the sequence randomly assigned based on a cross-over design: • Chrono Super PID then Generic Syringe-Gammanorm
Generic Syringe then Chrono Super PID - Gammanorm
OTHEREach patient will receive the study treatment using each of the two studied delivery devices according to the sequence randomly assigned based on a cross-over design: • Generic Syringe then Chrono Super PID-Gammanorm
Interventions
Each patient will receive the study treatment of Gammanorm using each of the two studied delivery devices according to the sequence randomly assigned based on a cross-over design: • pump and then syringe The use of automatic, programmable, compact pumps (such as CRONO SUPER PID) allows patients to remain mobile without interrupting their activities. Patients can infuse several sites simultaneously with infusion rates of up to 40 mL/h at 2 to 4 sites (abdomen, thighs, upper arms, lower back). Rapid and manual administration of SCIg using a syringe could therefore represent an alternative method by decreasing the duration of administration (around 10 minutes per injection at 1 or 2 sites simultaneously). The injection is self-administered by the patient. The infusion rate usually is 1 to 2 mL/min. The use of low viscosity products could facilitate injection
Each patient will receive the study treatment using each of the two studied delivery devices according to the sequence randomly assigned based on a cross-over design: • syringe and then pump. The use of automatic, programmable, compact pumps (such as CRONO SUPER PID) allows patients to remain mobile without interrupting their activities. Patients can infuse several sites simultaneously with infusion rates of up to 40 mL/h at 2 to 4 sites (abdomen, thighs, upper arms, lower back). Rapid and manual administration of SCIg using a syringe could therefore represent an alternative method by decreasing the duration of administration (around 10 minutes per injection at 1 or 2 sites simultaneously). The injection is self-administered by the patient. The infusion rate usually is 1 to 2 mL/min. The use of low viscosity products could facilitate injection
Eligibility Criteria
You may qualify if:
- Adult patients (≥ 18 years).
- Presenting with primary immunodeficiency.
- For whom the investigator decides to maintain immunoglobulin replacement therapy with subcutaneous injections of Gammanorm® 165 mg/mL at home.
- Freely given written informed consent from patient.
- Women of childbearing potential must have a negative result on a pregnancy test (human chorionic gonadotropine \[HCG\]-based assay) and need to practice contraception using a method of proven reliability for the duration of the study.
You may not qualify if:
- Participating in another interventional clinical study and receiving investigational medicinal product within three months before study entry.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Octapharmalead
Study Sites (12)
CampbelltownHospital
Campbelltown, NSW 2560, Australia
Canberra Hospital
Canberra, ACT 2605, Australia
University Medical Centre Freiburg
Freiburg im Breisgau, D-79106, Germany
Municipal Hospital "St. Georg"
Leipzig, D-04129, Germany
Azienda Ospedaliera di Padova, Allergologia ed Immunologia Clinica
Padua, 35128, Italy
Policlinic Umberto I - Universita di Roma "Sapienza", Clinical Immunology
Rome, 00161, Italy
University Hospitals Birmingham
Birmingham, B15 2GW, United Kingdom
University Hospital of Wales
Cardiff, CF144XW, United Kingdom
- The Royal London Hospital
London, E12ES, United Kingdom
The Royal Free
London, NW3 2QG, United Kingdom
John Radcliff Hospital
Oxford, OX3 9DU, United Kingdom
Derriford Hospital
Plymouth, PL6 8DH, United Kingdom
Related Publications (69)
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PMID: 21365217BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Klaus Warnatz, MD
Centre of Chronic Immunodeficiency, University Medical Centre Freiburg, Breisacher
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 1, 2015
First Posted
July 20, 2015
Study Start
July 29, 2015
Primary Completion
December 11, 2017
Study Completion
December 11, 2017
Last Updated
April 9, 2019
Record last verified: 2019-04