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''Evaluation of the efficacy of 'TRANS-DERMAL NITRATE' in reducing the severity of 'death-rattle' (i.e 'terminal lung secretions' ) in patients dying from end stage malignancy'' - n/a

''Evaluation of the efficacy of 'TRANS-DERMAL NITRATE' in reducing the severity of 'death-rattle' (i.e 'terminal lung secretions' ) in patients dying from end stage malignancy'' - n/a

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2007-004369-16-GB
Enrollment
Unknown
Registered
2007-10-15
Start date
2007-11-29
Completion date
Unknown
Last updated
2012-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

'Death-rattle' (i.e 'terminal lung secretions') in adult patients dying from end-stage malignancy

Interventions

Trade Name: TRANSIDERM NITRO 10 Product Name: TRANS-DERMAL NITRATE 10 Product Code: n/a Pharmaceutical Form: Transdermal patch INN or Proposed INN: n/a CAS Number: n/a Current Sponsor code: MJ/LPGB/12

Sponsors

St Raphael's Hospice, Surrey
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with advanced malignancy who enter the 'terminal phase' i.e (eligible for 'Integrated care pathway' for the dying) 2.Patients over 18 years of age Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: 1.Patients with Primary Brain Tumour 2.Patients with Cerebral Metastases 3.Patients with 'Motor Neurone Disease' 4.Patients with 'end-stage cardiac failure'

Design outcomes

Primary

MeasureTime frame
Secondary Objective: 1.Reduce the perception of the severity of 'death-rattle' by the patient's 'loved ones', thereby postively impact on bereavement 2.Reduce staff's perception of the severity of 'lung secretions', thereby minimise staff' distress 3.Reduce the requirement for frequent extra doses of the standard anti-secretory agent use or the need for increase of the 24 hour dose of same, thereby minimising dry mouth, 'thirst element' for the unconscious, dying patient 4.Reduce the requirement for the use of parenteral (i.e s/c,i/m or i/v) Furosemide;Primary end point(s): 1. Maximum noise level ( in dB ) of the 'death-rattle' at mid-day (tested using CASTLE GA 208 sound level meter)-average of 3 readings- 2. Relative's perception of the severity of ''death-rattle''--as mild; moderate; or severe 3. Clinical staff's perception of the severity of ''lung secretions''--as mild; moderate or severe;Main Objective: Evaluate the efficacy of 'TRANS-DERMAL NITRATE' in reducing the severity of 'death-rattle' ( i.e 'terminal lung secretions') in adult patients dying from end-stage malignancy

Countries

United Kingdom

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026