No registrations found.
ID
Source
Brief title
Health condition
Abnormal Uterine Bleeding
Sponsors and support
Intervention
Outcome measures
Primary outcome
Surgical re-intervention in Máxima MC in women with abnormal uterine bleeding who underwent Novasure treatment in 2018
Secondary outcome
- Patient characteristics: age, BMI, height and weight
- Time between Novasure and re-intervention
- Pre-existent Tubal ligation
- Pre-existent dysmenorrhea
- Uterine position
- Time and power ablation
- Analgesia (sedation, treatment room, Operating Room)
Background summary
Endometrial ablation using Novasure is a treatment in which the endometrium is removed in women with abnormal uterine bleeding. Unfortunately, in 10-20% of women, surgical re-intervention in the form of another ablation or even a hysterectomy is required because initial treatment has failed. For this reason, it is important to identify prognostic risk factors which are associated with treatment failure, and to continuously and conveniently evaluate clinical data in order to improve the effectiveness of Novasure endometrial ablation.
The current standard for real-world data extraction from the Electronic Health Record (EHR) is manual search and review of free text in EHR. This is an inefficient, time-consuming and laborious process, which is difficult to monitor and reproduce and, moreover, it contravenes the General Data Protection Regulation (GDPR). Clinical Data Collector (CDC) is a text mining software tool to collect structured and unstructured data from the EHR in a pseudonymised way through a search query. The search can be saved and reused, which increases verifiability. Data extraction with CDC has the additional advantage that only data that is relevant for the search query (minimizing data extraction) is automatically requested and pseudonymised (i.e. GDPR security). With the use of CDC, the efficiency of data extraction can be greatly improved. However, the validity of the extracted data depends on the quality of the CDC search. This search must take into account the different ways of registering in EHR by care professionals. Preparing a good search query in CDC can therefore be a challenge and must be critically evaluated.
In this study, we want to evaluate whether EHR data extraction with CDC to study the effectiveness of Novasure endometrial ablation is reliable compared to manual EHR data extraction.
Study objective
Data extraction with CDC to study the effectiveness of Novasure endometrial ablation is reliable compared to manual EHR data extraction
Study design
Primary outcome:
- Surgical reintervention measured during a follow-up of 2 years after Novasure endometrial ablation as recorded in the EHR by the healthcare professional.
Secondary outcomes as recorded in the EHR by the healthcare professional:
- Patient characteristics measured at the time of Novasure endometrial ablation. If not possible/available: measurement at a time point as close as possible to the intervention
- Time between Novasure endometrial ablation and re-intervention
- Pre-existent Tubal ligation (i.e. any time point before Novasure endometrial ablation)
- Pre-existent dysmenorrhea (i.e. any time point before Novasure endometrial ablation)
- Uterine position, preferably the last measurement before Novasure endometrial ablation
- Time and power ablation at the time of Novasure endometrial ablation
- Analgesia (sedation, treatment room, Operating Room) at the time of Novasure endometrial ablation
Intervention
Novasure endometrial ablation
Inclusion criteria
Woman who suffer from abnormal uterine bleeding and who previously underwent Novasure treatment in 2018 in Máxima MC
Exclusion criteria
Previous surgical intervention for heavy menstrual bleeding
Design
Recruitment
IPD sharing statement
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL9268 |
Other | Commissie Lokale Uitvoerbaarheid Máxima Medical Center : L20.188 |