PilBouTox® Project: Button Battery Poisoning From Data Collected by French Poison Control Centres (PILBOUTOX)
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03708250 |
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Recruitment Status :
Completed
First Posted : October 17, 2018
Last Update Posted : October 18, 2018
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| Condition or disease |
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| Button Battery Poisoning |
| Study Type : | Observational |
| Actual Enrollment : | 510 participants |
| Observational Model: | Case-Only |
| Time Perspective: | Prospective |
| Official Title: | PilBouTox® Project: Prospective and Descriptive Study About Button Battery Poisoning Performed on Data Collected by French Poison Control Centres (PCC) |
| Actual Study Start Date : | June 1, 2016 |
| Actual Primary Completion Date : | May 31, 2018 |
| Actual Study Completion Date : | May 31, 2018 |
- occurrence of a serious complication [ Time Frame: Baseline ]occurrence of a serious complication
- Need for surgery [ Time Frame: baseline ]Need for surgery
- Length of hospital stay [ Time Frame: baseline ]Length of hospital stay
- Death [ Time Frame: baseline ]Death
- Battery Size [ Time Frame: baseline ]Battery Size
- Battery Voltage [ Time Frame: baseline ]Battery Voltage
- Presence of Lying [ Time Frame: baseline ]Presence of Lying
- Length of Insertion [ Time Frame: baseline ]Length of Insertion
- Abnormalities at First Fibroscopy [ Time Frame: baseline ]Abnormalities at First Fibroscopy
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | Child, Adult, Older Adult |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
Any call that occurred during the period studied in a Poison Control Centre and concerning an exposure to a button cell regardless of the route of exposure, the age of the patient, and its symptomatology.
Exclusion Criteria:
Animal cases
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03708250
| France | |
| Centre Anti Poison | |
| Angers, France | |
| Centre Anti Poison | |
| Lille, France | |
| Centre Anti Poison | |
| Lyon, France | |
| Centre Anti Poison | |
| Marseille, France | |
| Centre Anti Poison | |
| Nancy, France | |
| Centre Anti Poison | |
| Paris, France | |
| Centre Anti Poison | |
| Strasbourg, France | |
| Centre Anti Poison | |
| Toulouse, France | |
| Responsible Party: | University Hospital, Bordeaux |
| ClinicalTrials.gov Identifier: | NCT03708250 |
| Other Study ID Numbers: |
CHUBX 2018/54 |
| First Posted: | October 17, 2018 Key Record Dates |
| Last Update Posted: | October 18, 2018 |
| Last Verified: | October 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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button battery intoxication oesophageal necrosis Poison Control Centre Poisoning |
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Poisoning Chemically-Induced Disorders |

