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Stentssms&FUSNCT01172158

SMS Reminder for Forgotten Ureteral Stents

An observational study of Stents, run by Dicle University at 1 site in Turkey (Türkiye).

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Ureteral stents has become an indispensable instrument for urology practice as a result of widespread use of endourological interventions. Removal of stents could be sometimes neglected by patients or physicians. Read more about this study

Who is it for?
Ages 1 year to 80 years
Conditions the study is for
Stents
How many people
250 participants
Where
1 siteTurkey (Türkiye)
Study dates
May 2010to Aug 2011
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 1 year to 80 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: First an institutional subscription agreement was signed between our university and a mobile phone cell company which is supporting SMS sending program. In the By making software plug-in to our hospital's patient follow up program, two programs were integrated. According to this integration, after stent insertion, in case of entering the numerical code corresponding of ''ureteral stent application'' procedure during the stage of epicrisis preparation, the patient follow up system warns the official recording the epicrisis to enter the stent removal time. Patient follow up system transfers this information to SMS sending program. After several weeks of the procedure, if the stent needs to be removed, the software automatically sends a warning message to the patient and the physician.

Who may be able to join

  • Patients who had ureteral stent insertion.

Who cannot join

  • Patients who did not want SMS message from us or want to give cell phone number.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Dicle University School of Medicine

    Diyarbakır

Other trials in Turkey (Türkiye)

About this study

Official title: A Solution for Medical and Legal Problems Arising From Forgotten Ureteral Stents: Reminder Short Message Service (SMS)

Ureteral stents has become an indispensable instrument for urology practice as a result of widespread use of endourological interventions. Removal of stents could be sometimes neglected by patients or physicians. This omission may lead to legal and medical problems for urologists, health institutions and also for patients. In this study, the investigators offer a computer program providing two sided recall to prevent this nasty complication with sending automatic message by short message service (SMS) to both the patient and the urologist.

Read the detailed description

In this study, first an institutional subscription agreement was signed between our university and a mobile phone cell company which is supporting SMS sending program. In the second step, by making software plug-in to our hospital's patient follow up program, two programs were integrated. According to this integration, after stent insertion, in case of entering the numerical code corresponding of ''ureteral stent application'' procedure during the stage of epicrisis preparation, the patient follow up system warns the official recording the epicrisis to enter the stent removal time. Patient follow up system transfers this information to SMS sending program. After several weeks of the procedure, if the stent needs to be removed, the software automatically sends a warning message to the patient and the physician. If the patients attends to urology department and undergoes stent removal, the official enters the code of "endoscopic stent removal" to the patient follow-up program. Then the program stops to send warning message.

By the software plug-in to patient follow up program, SMS sending was made mandatory not to forget or skip none of the patients during the epicrisis writing procedure.

Conditions
Stents
Keywords
forgotten ureteral stents, SMS Reminder

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT01172158
Study groupRoleWhat they receive
Forgotten ureteral stentsNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. A solution for medical and legal problems arising from forgotten ureteral stents: Reminder Short Message Service (SMS)

    Primary Outcome Measure will be evaluated with;

    1. Number of the patients who admitted for stent removal will be compared with the patients who did not admit. So the effectivity of the SMS sending proram will be evaluated.
    2. The percentage of complication of forgotten ureteral stent will be calculated. And this rate will be compared with the previous rate of same department and the rates reported in the literature.
    3. Patient satisfaction surveys
    4. The time of the patients admitted. The data obtained from this study will be compared with previous data.

    Measured: five months

Secondary outcomes (1)
  1. SMS Reminder for Forgotten Ureteral Stents

    Secondary, this practice can be prevalent in all hospitals at the our country.

    Measured: one year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Jul 2010 (estimated)
  2. Study startMay 2010
  3. Primary completionOct 2010 (estimated)
  4. Study completionAug 2011 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Prospective
Enrolment
250 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01172158
Sponsor's protocol ID
1-Dicle University
Acronym
sms&FUS
Status last verified
Jul 2010
First submitted
29 Jun 2010
Last updated
29 Jul 2010
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Stents, run by Dicle University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 29 Jul 2010. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

A solution for medical and legal problems arising from forgotten ureteral stents: Reminder Short Message Service (SMS) (time frame: five months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Jul 2010.

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