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NCT03695081
Patient Pathway Pharmacist - Optimal Drug-related Care
NA trial testing Patient Pathway Pharmacist intervention in Hip Fractures in 60 participants. Completed in 28 June 2023.
15 June 2019
Quick facts
| Lead sponsor | Sykehuset i Vestfold HF |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | single group |
| Masking | none |
| Primary purpose | supportive care |
| Enrollment | 60 |
| Start date | 3 September 2018 |
| Primary completion | 15 June 2019 |
| Estimated completion | 28 June 2023 |
| Sites | 1 location across Norway |
Drugs / interventions tested
- Patient Pathway Pharmacist intervention
Conditions studied
- Hip Fractures — all drugs for Hip Fractures →
- Aging — all drugs for Aging →
- Patient Fall — all drugs for Patient Fall →
Sponsor
Sykehuset i Vestfold HF — full company profile →
Who can join
18 and older, any sex, with Hip Fractures or Aging. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Medication errors represent the most common cause of patient injury and one of the most frequently reported health related deviation in Norway. The addition of a dedicated clinical pharmacist throughout the hip fracture patient pathway (patient pathway pharmacist) is believed to improve patient safety and ensure optimal drug-related patient care. The pharmacist will perform medication reconciliation at admission to hospital, medication review after surgery and assist physicians with discharge summary. Six weeks after discharge the patient pathway pharmacist will perform a second drug reconciliation and medication review. This study will assess the pharmacists' place and specific tasks in the patient pathway, describe areas where the pharmacist contribute to increased quality of care and assess the benefits and/or disadvantages experienced with introducing a patient pathway pharmacist. The estimated number of patients included is 60. Current practice will be determined by investigating the last 50 patients' medical record and a questionnaire to health care professionals involved in treatment of hip fracture patients. Data from medication reconciliation and drug review will be collected and compared to current practice. After the inclusion period, focus group surveys and/or semi-structured interviews will be executed to describe the perceived improvement in the quality of care. Primary endpoints are: 1) Medication reconciliation score at admission 2) Number of inappropriate drugs for elderly 3) Discharge summary score 4) Discharge summaries following procedure. Secondary endpoints are readmissions and mortality after 30 and 90 days. Qualitative endpoints: 1) Health care professionals experience of current drug-related practice 2) Experienced advantages and disadvantages of a patient pathway pharmacist.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Medication review in hospitalised patients to reduce morbidity and mortality.
Bülow C, Clausen SS, Lundh A, Christensen M. · · 2023 · cited 37× · PMID 36688482 · DOI 10.1002/14651858.cd008986.pub4 -
Clinical pharmacist intervention to improve medication safety for hip fracture patients through secondary and primary care settings: a nonrandomised controlled trial.
Henriksen BT, Krogseth M, Andersen RD, Davies MN, et al · · 2023 · cited 10× · PMID 37312222 · DOI 10.1186/s13018-023-03906-2
Verify or expand the search:
- PubMed search for NCT03695081
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Hip Fractures
Currently open trials in the same condition.
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- NCT06455813 — What Laxative Should be Used After Hip Fracture Surgery? · Phase 4 · recruiting
Other Sykehuset i Vestfold HF trials
Trials by the same sponsor.
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- NCT06045741 — Virtual Reality - A New Vision on Pain · completed
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03695081 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Sykehuset i Vestfold HF
- Last refreshed: 29 June 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03695081.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing