Trials / Unknown
UnknownNCT02957877
LMWH Infusion as Anticoagulation for Home HD
Low-molecular Heparin Infusion as Anticoagulation for Nocturnal Home Hemodialysis
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 12 (estimated)
- Sponsor
- Alice Ho Miu Ling Nethersole Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
There is a lack of data in the literature about the use of low-molecular weight heparin (LMWH) as anticoagulation for nocturnal home hemodialysis (NHHD). This study aims to evaluate the efficacy and safety of LMWH, administered by infusion method, as compared to unfractionated heparin as anticoagulation for NHHD treatment.
Detailed description
Low-molecular weight heparin (LMWH) and unfractionated heparin (UFH) are established systemic anticoagulants for the patients who receive conventional thrice-weekly hemodialysis in absence of significant bleeding risk. For the patients who undergo nocturnal home hemodialysis (NHHD), LMWH is seldom utilized because of the need of an additional bolus injection during a long dialysis treatment, which is impractical as the patients are sleeping during hemodialysis. Moreover, there is a potential risk of LMWH accumulation due to its longer half-life. As there is a paucity of data in the literature on the use of LMWH for NHHD treatment, this trial is conducted to assess the safety and efficacy of LMWH, administered by infusion method, in this particular group of dialysis patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Nadroparin | A nadroparin infusion regimen (loading dose of 35 IU/kg, followed by 10 IU/kg per hour for 6 hours) is administered as anticoagulation during the 8-hour hemodialysis. |
| DRUG | Unfractionated heparin | The individualized unfractionated heparin infusion regimen currently employed by the recruited patients in their home dialysis treatment is administered as anticoagulation during the 8-hour hemodialysis. |
Timeline
- Start date
- 2016-03-01
- Primary completion
- 2018-05-01
- Completion
- 2018-05-01
- First posted
- 2016-11-08
- Last updated
- 2016-11-08
Locations
1 site across 1 country: Hong Kong
Source: ClinicalTrials.gov record NCT02957877. Inclusion in this directory is not an endorsement.