Hyperparathyroidism, Insomnia, Ostalgia, Refractory Pruritus
Conditions
Keywords
hemodialysis, hyperparathyroidism, refractory pruritus, ostalgia, insomnia, CVD incidence, life quality
Brief summary
A prospective, randomized, controlled open clinic trial to evaluate the effect and safety of combination of conventional hemodialysis(HD) and hemoperfusion(HP) on middle molecules removal and complications improvement in long-term maintenance hemodialysis (MHD) patients. There are two phases of study for each subject. Phase 1 (screening phase). During this phase, each potential subject will be evaluated to determine if he/she is eligible for the study. Phase 2 (intervention phase). Each subject will be randomly allocated to HD+HP(HA130 once per week) group ,HD+HP(HA330 once per week) group and HD group. The follow-up duration was 3 months.
Detailed description
All patients recruited from these centers who met the inclusion criteria were randomly allocated to HD+HP(HA130 once per week) group ,HD+HP(HA330 once per week) group and HD group. The follow-up duration was 3 months. Hemoperfusion is performed by HA130 or HA330 resin adsorbents. Blood flow is 200ml/min，dialysate flow is 500ml/min， hemodialysis and hemoperfusion last for 2.5h，continue HD after removing the adsorbent to complete 4 hours'treatment.Heparin for anticoagulation ：first pulse 0.5-1mg/kg ，appending 8-10mg/h. Primary endpoint is the improvement of the clinic symptoms, meanwhile secondary endpoint is serum β2MG、iPTH、CRP、ADMA、BMP2 decrease compared with the baseline, life quality, nutrition condition, and cardiovascular (CVD) incidence.
Interventions
OTHERhemodialysis only
hemodialysis treatment only
OTHERhemodialysis plus hemoperfusion(HA330)
combination of hemodialysis and hemoperfusion (HA330) treatment
OTHERhemodialysis plus hemoperfusion(HA130)
combination of hemodialysis and hemoperfusion (HA130) treatment
Sponsors
Sun Yat-sen University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
16 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* Willingness to sign an informed consent * Stable haemodialysis treatment for more than 3 months, undergoing 2 to 3 times haemodialysis a week for 4 to 5 hours per session * middle or large molecules retention defined as immunoreactive parathyroid hormone (iPTH) \> 400 pg/mL, β2MG\>5000 pg/ml、CRP\>10mg/l. * Refractory pruritus, carpal tunnel syndrome, restless leg syndrome, hyperparathyroidism or other refratory complications.
Exclusion criteria
* Incapable or reluctant to sign the informed consent or comply the schedule. * platelet (PLT) count\<60×109/L or disturbance in coagulation, tendency of severe bleeding or acute bleeding. * Severe hypotension and heart or lung insufficiency * Known hypersensitive or contradiction or intolerance to dialyzer or adsorbents * Attend to other clinic trial now or in recent 30 days
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the longitudinal changes of itching | every week, up to 12 weeks. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| the longitudinal changes of serum middle molecules of iPTH concentrations | every week,up to 12 weeks. | The serum concentration of iPTH will be measured using ELISA method |
| the longitudinal changes of serum middle molecules of CRP concentrations | every week,up to 12 weeks. | The serum concentration of CRP will be measured using ELISA method |
| the longitudinal changes of serum middle molecules of β2MG concentrations | every week,up to 12 weeks. | The serum concentration of β2MG will be measured using ELISA method |
| the longitudinal changes of serum middle molecules of BMP2concentrations | every week,up to 12 weeks. | The serum concentration of BMP2 will be measured using ELISA method |
| the longitudinal changes of the nutritional status | every week,up to 12 weeks. | The nutritional status was evaluated using the serum level of albumin, the subjective global assessment score and BMI. The serum level of albumin will measured using the blood analysis biochemical analyzer, the subjective global assessment score will measured using the SGA scale and the BMI will measured through the physical examination and calculated by weight (kg)/height2 (m2). |
| the longitudinal changes of serum middle molecules of ADMA concentrations | every week,up to 12 weeks. | The serum concentration of ADMA will be measured using ELISA method |
Countries
China
Outcome results
None listed