Pain Medication After Ambulatory Surgery
Adequacy and Adverse Effects of Pain Medication After Ambulatory Surgery, Observational Study
Studieöversikt
Status
Detaljerad beskrivning
After informed consent, all patients operated as ambulatory surgery patients during the study period are given a letter interview for pain, pain medication and symptom follow up. They are also given a return envelope (with paid postal fee) to return the interview.
Based on the results of the first interview phase, our pain medication practice is reconsidered by anesthetists and surgeons to create a standard operating protocol for pain medication. The standard operating protocol is informed to personnel. Then, patient interview phase is repeated for another 3 months.
Then, investigators continue with a pilot study on using a mobile phone app in evaluating patients pain, sufficient pain medication and adverse effects. All patient with informed consent, suitable mobile phone, and willing to use it for reporting pain for hospital personnel are contacted via the mobile app. Other patients operated during that study period are interviewed by either letter interview or phone interview. Investigators try to estimate whether mobile apps are suitable for pain and medication follow-up.
Studietyp
Inskrivning (Faktisk)
Kontakter och platser
Studieorter
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Vantaa, Finland, 00029
- Helsinki University (Central) Hospital, Peijas Hospital
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Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Testmetod
Studera befolkning
Beskrivning
Inclusion Criteria:
All plenipotentiary patients, operated as ambulatory surgery patients in our clinic during the study period, with informed consent
Exclusion Criteria:
We do not accept patients, who are not plenipotentiary (minor, incompetent, prisoners, conscript in military service) or do not understand finnish or swedish written information
Studieplan
Hur är studien utformad?
Designdetaljer
Kohorter och interventioner
Grupp / Kohort |
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Current practice group
All plenipotentiary ambulatory surgery patients, with informed consent, during the three month study period
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Standard operating protocol group
All plenipotentiary ambulatory surgery patients, with informed consent, during the three month study period after creating and informing standardized operating protocol
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Mobile phone app group
All plenipotentiary ambulatory surgery patients during the three month study period with informed consent to use mobile phone app in assesment of pain and pain medication
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
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Medication
Tidsram: up to two days after surgery
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all pain medication used (reported By the patient)
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up to two days after surgery
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Pain
Tidsram: up to two days after surgery
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Pain assessed By the patient By numerical rating scale 0-10
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up to two days after surgery
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Adverse effects
Tidsram: up to two days after surgery
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Adverse effects of the pain medication, study questions
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up to two days after surgery
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Sufficiency of pain medication
Tidsram: up to two days after surgery
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Whether the pain medication used was sufficient or not, study questions
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up to two days after surgery
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Samarbetspartners och utredare
Utredare
- Huvudutredare: Elina Reponen, MD/PhD, Senior physician, Deputy Chief of Department
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- HUS235/2017
Plan för individuella deltagardata (IPD)
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Läkemedels- och apparatinformation, studiedokument
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