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Non-interventional trial on the postoperative use of bromelain tablets hysan in an ENT setting

Non-interventional trial on the postoperative use of bromelain tablets hysan in an ENT setting - BROHNO-2015

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00010112
Enrollment
120
Registered
2016-03-01
Start date
2016-03-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

surgeries in ENT, not prespecified

Interventions

Group 1: - Patients = 12 Jahre - Surgery in ENT setting - doctor's decision to prescribe bromelain tablets hysan is Independent from decistion to include the Patient into the study

Sponsors

URSAPHARM Arzneimittel GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to No maximum

Inclusion criteria

Inclusion criteria: - Patients = 12 Jahre - Surgery in ENT setting - doctor's decision to prescribe bromelain tablets hysan is Independent from decistion to include the Patient into the study

Exclusion criteria

Exclusion criteria: Due to the non-interventional character of the study, no exclusion criteria are predefined. Contraindications and interactions as described in SPC must be considered.

Design outcomes

Primary

MeasureTime frame
Efficacy: - Change in clinical symptoms such as pain, oedema, inflammation during the treatment period. - Global judgement of the doctor on the efficacy of the treatment -Reduction in use of analgetics - Continuation of therapy/ planned reapplication of bromelain tablets hysan® Safety: incidence of adverse reactions under treatment judgement on tolerability of the treatment

Secondary

MeasureTime frame
descriptive Analysis of data, therefore there is no separate considering of Primary and secondary outcomes. All outcomes are listed in section Primary Outcome.

Countries

Germany

Contacts

Public ContactPeter Meiser

URSAPHARM Arzneimittel GmbH

p.meiser@ursapharm.de06805-9292-0

Outcome results

None listed

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